Canonical Allele Identifier: CA191701681
Gene:

Linked Data

dbSNP Id: rs192957320
gnomAD v2: 9-25551221-T-C
gnomAD v3: 9-25551223-T-C
gnomAD v4: 9-25551223-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551223T>C , CM000671.2:g.25551223T>C GRCh38
NC_000009.11:g.25551221T>C , CM000671.1:g.25551221T>C GRCh37
NC_000009.10:g.25541221T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-651A>G
XR_929525.2:n.674-651A>G