Canonical Allele Identifier: CA1502607303
Gene:

Linked Data

dbSNP Id: rs1732905202

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748416T>A , CM000666.2:g.148748416T>A GRCh38
NC_000004.11:g.149669568T>A , CM000666.1:g.149669568T>A GRCh37
NC_000004.10:g.149889018T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741441.1:n.1746-118341T>A