Canonical Allele Identifier: CA1233224675
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.773329C= , CM000664.2:g.773329C= GRCh38
NC_000002.11:g.773329C= , CM000664.1:g.773329C= GRCh37
NC_000002.10:g.763329C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510439.1:c.-24-3507C= XP_011508741.1:n.-24-3507C=
XM_011510440.1:c.-24-3507C= XP_011508742.1:n.-24-3507C=
XM_011510441.1:c.-24-3507C= XP_011508743.1:n.-24-3507C=
XM_011510442.1:c.-24-3507C= XP_011508744.1:n.-24-3507C=
XM_011510443.1:c.-24-3507C= XP_011508745.1:n.-24-3507C=
XR_922708.1:n.4001-3507C=