Canonical Allele Identifier: CA1481405427
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499621G= , CM000666.2:g.102499621G= GRCh38
NC_000004.11:g.103420778G= , CM000666.1:g.103420778G= GRCh37
NC_000004.10:g.103639810G= NCBI36
NG_050628.1:g.3293G=

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+1628C= XP_011530769.1:n.643+1628C=
NR_136202.1:n.48+2818C=