Canonical Allele Identifier: CA1216113099
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121737C= , CM000663.2:g.193121737C= GRCh38
NC_000001.10:g.193090867C= , CM000663.1:g.193090867C= GRCh37
NC_000001.9:g.191357490C= NCBI36
NG_012691.1:g.4780C= , LRG_507:g.4780C=

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1920G=