Canonical Allele Identifier: CA862568186
Gene:

Linked Data

dbSNP Id: rs1302999527
gnomAD v3: 9-25551401-T-C
gnomAD v4: 9-25551401-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551401T>C , CM000671.2:g.25551401T>C GRCh38
NC_000009.11:g.25551399T>C , CM000671.1:g.25551399T>C GRCh37
NC_000009.10:g.25541399T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-829A>G
XR_929525.2:n.674-829A>G