Canonical Allele Identifier: CA197410885
Gene:

Linked Data

dbSNP Id: rs56064613

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928260G>A , CM000671.2:g.104928260G>A GRCh38
NC_000009.11:g.107690541G>A , CM000671.1:g.107690541G>A GRCh37
NC_000009.10:g.106730362G>A NCBI36
NG_007981.1:g.4896C>T

Transcript Alleles

HGVS Amino-acid change
XR_930204.1:n.734+350G>A
XR_930204.2:n.115+350G>A