Canonical Allele Identifier: CA2378395206
Community Standard Title: NC_000021.9:g.15542586G=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.15542586G= , CM000683.2:g.15542586G= GRCh38
NC_000021.8:g.16914905G= , CM000683.1:g.16914905G= GRCh37
NC_000021.7:g.15836776G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754972.1:n.403-15863C=