Canonical Allele Identifier: CA1141880933
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800672G= , CM000663.2:g.192800672G= GRCh38
NC_000001.10:g.192769802G= , CM000663.1:g.192769802G= GRCh37
NC_000001.9:g.191036425G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.102G=