Canonical Allele Identifier: CA1839056702
Gene:

Linked Data

dbSNP Id: rs1823378163

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21756018C>G , CM000671.2:g.21756018C>G GRCh38
NC_000009.11:g.21756017C>G , CM000671.1:g.21756017C>G GRCh37
NC_000009.10:g.21746017C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11807G>C