Canonical Allele Identifier: CA16132435
Gene:

Linked Data

dbSNP Id: rs35964523
gnomAD v2: 3-898661-C-T
gnomAD v3: 3-856978-C-T
gnomAD v4: 3-856978-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.856978C>T , CM000665.2:g.856978C>T GRCh38
NC_000003.11:g.898661C>T , CM000665.1:g.898661C>T GRCh37
NC_000003.10:g.873661C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001740584.1:n.1837C>T