Canonical Allele Identifier: CA775632392
Gene:

Linked Data

dbSNP Id: rs1371857124
gnomAD v3: 17-8137671-A-C
gnomAD v4: 17-8137671-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137671A>C , CM000679.2:g.8137671A>C GRCh38
NC_000017.10:g.8040989A>C , CM000679.1:g.8040989A>C GRCh37
NC_000017.9:g.7981714A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934202.1:n.183-1178A>C
XR_934203.1:n.70-1806A>C
XR_934202.2:n.414-1178A>C