Canonical Allele Identifier: CA1821941772
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.134866916T>A , CM000670.2:g.134866916T>A GRCh38
NC_000008.10:g.135879159T>A , CM000670.1:g.135879159T>A GRCh37
NC_000008.9:g.135948341T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125427.1:n.1697-14268T>A