Canonical Allele Identifier: CA1839056670
Gene:

Linked Data

dbSNP Id: rs1823377097

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21755953T>C , CM000671.2:g.21755953T>C GRCh38
NC_000009.11:g.21755952T>C , CM000671.1:g.21755952T>C GRCh37
NC_000009.10:g.21745952T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11872A>G