Canonical Allele Identifier: CA1216113162
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121828G= , CM000663.2:g.193121828G= GRCh38
NC_000001.10:g.193090958G= , CM000663.1:g.193090958G= GRCh37
NC_000001.9:g.191357581G= NCBI36
NG_012691.1:g.4871G= , LRG_507:g.4871G=

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1829C=