Canonical Allele Identifier: CA156301718
Gene:

Linked Data

dbSNP Id: rs1051085337
gnomAD v3: 7-26605733-T-A
gnomAD v4: 7-26605733-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26605733T>A , CM000669.2:g.26605733T>A GRCh38
NC_000007.13:g.26645352T>A , CM000669.1:g.26645352T>A GRCh37
NC_000007.12:g.26611877T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927131.1:n.1118-6363A>T
XR_927131.2:n.1186-6363A>T