Canonical Allele Identifier: CA1216113092
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121729C= , CM000663.2:g.193121729C= GRCh38
NC_000001.10:g.193090859C= , CM000663.1:g.193090859C= GRCh37
NC_000001.9:g.191357482C= NCBI36
NG_012691.1:g.4772C= , LRG_507:g.4772C=

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1928G=