Canonical Allele Identifier: CA1481407055
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501012G= , CM000666.2:g.102501012G= GRCh38
NC_000004.11:g.103422169G= , CM000666.1:g.103422169G= GRCh37
NC_000004.10:g.103641201G= NCBI36
NG_050628.1:g.4684G=

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+237C= XP_011530769.1:n.643+237C=
NR_136202.1:n.48+1427C=