Canonical Allele Identifier: CA1481406866
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500910G= , CM000666.2:g.102500910G= GRCh38
NC_000004.11:g.103422067G= , CM000666.1:g.103422067G= GRCh37
NC_000004.10:g.103641099G= NCBI36
NG_050628.1:g.4582G=

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+339C= XP_011530769.1:n.643+339C=
NR_136202.1:n.48+1529C=