Canonical Allele Identifier: CA1233617132
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1553992C= , CM000664.2:g.1553992C= GRCh38
NC_000002.11:g.1557764C= , CM000664.1:g.1557764C= GRCh37
NC_000002.10:g.1536771C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510447.1:c.-1181C= XP_011508749.1:n.-1181C=
XM_011510448.1:c.-1181C= XP_011508750.1:n.-1181C=
XR_922720.1:n.85+2506G=
XM_017005455.1:c.-1181C= XP_016860944.1:n.-1181C=
NR_168373.1:n.746-178C=