Canonical Allele Identifier: CA981245800
Gene:

Linked Data

dbSNP Id: rs1981895053
gnomAD v3: 17-8137672-T-C
gnomAD v4: 17-8137672-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137672T>C , CM000679.2:g.8137672T>C GRCh38
NC_000017.10:g.8040990T>C , CM000679.1:g.8040990T>C GRCh37
NC_000017.9:g.7981715T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934202.1:n.183-1177T>C
XR_934203.1:n.70-1805T>C
XR_934202.2:n.414-1177T>C