Canonical Allele Identifier: CA1216113066
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121695C= , CM000663.2:g.193121695C= GRCh38
NC_000001.10:g.193090825C= , CM000663.1:g.193090825C= GRCh37
NC_000001.9:g.191357448C= NCBI36
NG_012691.1:g.4738C= , LRG_507:g.4738C=

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1962G=