Canonical Allele Identifier: CA1374121545
Gene:

Linked Data

dbSNP Id: rs1704106491

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266756A>T , CM000665.2:g.72266756A>T GRCh38
NC_000003.11:g.72315907A>T , CM000665.1:g.72315907A>T GRCh37
NC_000003.10:g.72398597A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8352T>A