Canonical Allele Identifier: CA26899188
Gene:

Linked Data

dbSNP Id: rs767171804
gnomAD v2: 1-95029607-T-A
gnomAD v3: 1-94564051-T-A
gnomAD v4: 1-94564051-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564051T>A , CM000663.2:g.94564051T>A GRCh38
NC_000001.10:g.95029607T>A , CM000663.1:g.95029607T>A GRCh37
NC_000001.9:g.94802195T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+438T>A