Canonical Allele Identifier: CA163625039
Gene:

Linked Data

dbSNP Id: rs776665099
gnomAD v3: 7-97388450-T-C
gnomAD v4: 7-97388450-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388450T>C , CM000669.2:g.97388450T>C GRCh38
NC_000007.13:g.97017762T>C , CM000669.1:g.97017762T>C GRCh37
NC_000007.12:g.96855698T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59803A>G