Canonical Allele Identifier: CA26899184
Gene:

Linked Data

dbSNP Id: rs545790529
gnomAD v3: 1-94564048-T-C
gnomAD v4: 1-94564048-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564048T>C , CM000663.2:g.94564048T>C GRCh38
NC_000001.10:g.95029604T>C , CM000663.1:g.95029604T>C GRCh37
NC_000001.9:g.94802192T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+435T>C