Canonical Allele Identifier: CA1181633484
Gene:

Linked Data

dbSNP Id: rs1652358469

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564059A>T , CM000663.2:g.94564059A>T GRCh38
NC_000001.10:g.95029615A>T , CM000663.1:g.95029615A>T GRCh37
NC_000001.9:g.94802203A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+446A>T