Canonical Allele Identifier: CA1143126001
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800600A= , CM000663.2:g.192800600A= GRCh38
NC_000001.10:g.192769730A= , CM000663.1:g.192769730A= GRCh37
NC_000001.9:g.191036353A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.30A=