Canonical Allele Identifier: CA1573933686
Gene:

Linked Data

dbSNP Id: rs1780063097

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660983G>T , CM000667.2:g.113660983G>T GRCh38
NC_000005.9:g.112996680G>T , CM000667.1:g.112996680G>T GRCh37
NC_000005.8:g.113024579G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27619G>T