Canonical Allele Identifier: CA1481407158
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501096G= , CM000666.2:g.102501096G= GRCh38
NC_000004.11:g.103422253G= , CM000666.1:g.103422253G= GRCh37
NC_000004.10:g.103641285G= NCBI36
NG_050628.1:g.4768G=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+153C= XP_011530769.1:n.643+153C=
NR_136202.1:n.48+1343C=