Canonical Allele Identifier: CA71034092
Gene:

Linked Data

dbSNP Id: rs567451011
gnomAD v3: 3-18975794-C-T
gnomAD v4: 3-18975794-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.18975794C>T , CM000665.2:g.18975794C>T GRCh38
NC_000003.11:g.19017286C>T , CM000665.1:g.19017286C>T GRCh37
NC_000003.10:g.18992290C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940638.1:n.437+7756G>A
XR_001740612.1:n.774+7756G>A
XR_001740613.1:n.303+9387C>T
XR_001740614.1:n.303+9387C>T
XR_001740615.1:n.304+9387C>T
XR_001740616.1:n.304+9387C>T