Canonical Allele Identifier: CA1795570416
Gene:

Linked Data

dbSNP Id: rs1275253352

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.77413716C>G , CM000670.2:g.77413716C>G GRCh38
NC_000008.10:g.78325952C>G , CM000670.1:g.78325952C>G GRCh37
NC_000008.9:g.78488507C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929071.1:n.231-4962C>G
XR_001745963.1:n.191-4962C>G