Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 2:128180895 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM004278

Most severe consequence
Clinical significance

Synonyms

LSDB 17282

This variation has 13 HGVS names - click the plus to show

2:g.128180895A>C
ENST00000402125.2:c.31A>C
ENSP00000384225.2:p.His11Pro
ENST00000409048.1:c.548A>C
ENSP00000386679.1:p.His183Pro
ENST00000464089.1:n.32A>C
ENST00000453608.2:c.611A>C
ENSP00000404030.2:p.His204Pro
ENST00000422777.3:c.446A>C
ENSP00000409543.3:p.His149Pro
ENST00000234071.3:c.446A>C
ENSP00000234071.3:p.His149Pro
ENST00000442644.1:c.401-12A>C

Variation displays