Canonical Allele Identifier: CA1146388980
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121898G= , CM000663.2:g.193121898G= GRCh38
NC_000001.10:g.193091028G= , CM000663.1:g.193091028G= GRCh37
NC_000001.9:g.191357651G= NCBI36
NG_012691.1:g.4941G= , LRG_507:g.4941G=

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1759C=