Canonical Allele Identifier: CA2838211150
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2569975A>T , CM000663.2:g.2569975A>T GRCh38
NC_000001.10:g.2501414A>T , CM000663.1:g.2501414A>T GRCh37
NC_000001.9:g.2491274A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121638.1:n.71+3370A>T
XR_946834.1:n.2021A>T