Canonical Allele Identifier: CA1216113119
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121769T= , CM000663.2:g.193121769T= GRCh38
NC_000001.10:g.193090899T= , CM000663.1:g.193090899T= GRCh37
NC_000001.9:g.191357522T= NCBI36
NG_012691.1:g.4812T= , LRG_507:g.4812T=

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1888A=