Canonical Allele Identifier: CA1149683798
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2567457C= , CM000663.2:g.2567457C= GRCh38
NC_000001.10:g.2498896C= , CM000663.1:g.2498896C= GRCh37
NC_000001.9:g.2475522G= NCBI36
NG_047096.1:g.16093C=

Transcript Alleles

HGVS Amino-acid change
NR_121638.1:n.71+852C=