Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 2:26482441 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM024258

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

2:g.26482441A>G
ENST00000403946.5:c.1544T>C
ENSP00000385255.3:p.Ile515Thr
ENST00000272371.4:c.1544T>C
ENSP00000272371.2:p.Ile515Thr

Variation displays