Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 2:241767734 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM050362

Most severe consequence
Clinical significance

Synonyms

LSDB 16166

This variation has 15 HGVS names - click the plus to show

2:g.241767734T>C
ENST00000445308.1:c.727T>C
ENSP00000387479.1:p.Val243Ala
ENST00000612819.1:c.*172T>C
ENST00000473126.1:n.530T>C
ENST00000321264.5:c.1331T>C
ENSP00000315351.4:p.Val444Ala
ENST00000610344.1:c.*175T>C
ENST00000468064.2:n.1221T>C
ENST00000403782.2:c.929T>C
ENSP00000384723.1:p.Val310Ala
ENST00000400769.3:c.*81T>C
ENST00000436747.2:c.*2567T>C
ENST00000470343.2:n.812T>C
ENST00000486953.2:n.1155T>C

Variation displays