Canonical Allele Identifier: CA54965502
Gene:

Linked Data

dbSNP Id: rs886561564

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122369169T>G , CM000664.2:g.122369169T>G GRCh38
NC_000002.11:g.123126745T>G , CM000664.1:g.123126745T>G GRCh37
NC_000002.10:g.122843215T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-23794T>G
XR_001739684.1:n.556-23794T>G