Canonical Allele Identifier: CA1870932995
Gene:

Linked Data

dbSNP Id: rs1826975016

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092890G>C , CM000671.2:g.108092890G>C GRCh38
NC_000009.11:g.110855171G>C , CM000671.1:g.110855171G>C GRCh37
NC_000009.10:g.109894992G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930239.1:n.461-39596C>G
XR_001746881.1:n.668-39596C>G
XR_001746882.1:n.668-39596C>G