Canonical Allele Identifier: CA2718984875
Gene:

Linked Data

dbSNP Id: rs2118861903

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21756012A>G , CM000671.2:g.21756012A>G GRCh38
NC_000009.11:g.21756011A>G , CM000671.1:g.21756011A>G GRCh37
NC_000009.10:g.21746011A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746563.2:n.163+11813T>C