Canonical Allele Identifier: CA1147177347
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800698G= , CM000663.2:g.192800698G= GRCh38
NC_000001.10:g.192769828G= , CM000663.1:g.192769828G= GRCh37
NC_000001.9:g.191036451G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.128G=