Canonical Allele Identifier: CA587286382
Gene:

Linked Data

dbSNP Id: rs1457117362
gnomAD v2: 9-25551454-A-G
gnomAD v3: 9-25551456-A-G
gnomAD v4: 9-25551456-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551456A>G , CM000671.2:g.25551456A>G GRCh38
NC_000009.11:g.25551454A>G , CM000671.1:g.25551454A>G GRCh37
NC_000009.10:g.25541454A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-884T>C
XR_929525.2:n.674-884T>C