Canonical Allele Identifier: CA858083895
Gene:

Linked Data

dbSNP Id: rs1398958317

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928271A>G , CM000671.2:g.104928271A>G GRCh38
NC_000009.11:g.107690552A>G , CM000671.1:g.107690552A>G GRCh37
NC_000009.10:g.106730373A>G NCBI36
NG_007981.1:g.4885T>C

Transcript Alleles

HGVS Amino-acid change
XR_930204.1:n.734+361A>G
XR_930204.2:n.115+361A>G