Canonical Allele Identifier: CA1841175389
Gene:

Linked Data

dbSNP Id: rs1819671969

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551089T>G , CM000671.2:g.25551089T>G GRCh38
NC_000009.11:g.25551087T>G , CM000671.1:g.25551087T>G GRCh37
NC_000009.10:g.25541087T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-517A>C
XR_929525.2:n.674-517A>C