Canonical Allele Identifier: CA1870932937
Gene:

Linked Data

dbSNP Id: rs1826972656

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092810T>C , CM000671.2:g.108092810T>C GRCh38
NC_000009.11:g.110855091T>C , CM000671.1:g.110855091T>C GRCh37
NC_000009.10:g.109894912T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930239.1:n.461-39516A>G
XR_001746881.1:n.668-39516A>G
XR_001746882.1:n.668-39516A>G