Canonical Allele Identifier: CA1216113091
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121728A= , CM000663.2:g.193121728A= GRCh38
NC_000001.10:g.193090858A= , CM000663.1:g.193090858A= GRCh37
NC_000001.9:g.191357481A= NCBI36
NG_012691.1:g.4771A= , LRG_507:g.4771A=

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1929T=