Canonical Allele Identifier: CA1233617214
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1554170G= , CM000664.2:g.1554170G= GRCh38
NC_000002.11:g.1557942G= , CM000664.1:g.1557942G= GRCh37
NC_000002.10:g.1536949G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510447.1:c.-1003G= XP_011508749.1:n.-1003G=
XM_011510448.1:c.-1003G= XP_011508750.1:n.-1003G=
XR_922720.1:n.85+2328C=
XM_017005455.1:c.-1003G= XP_016860944.1:n.-1003G=
NR_168373.1:n.746G=