Canonical Allele Identifier: CA802120371
Gene:

Linked Data

dbSNP Id: rs1325429859

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660939A>T , CM000667.2:g.113660939A>T GRCh38
NC_000005.9:g.112996636A>T , CM000667.1:g.112996636A>T GRCh37
NC_000005.8:g.113024535A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27575A>T