Canonical Allele Identifier: CA1104780626
Gene:

Linked Data

dbSNP Id: rs1646579950
gnomAD v3: 7-97388471-T-A
gnomAD v4: 7-97388471-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388471T>A , CM000669.2:g.97388471T>A GRCh38
NC_000007.13:g.97017783T>A , CM000669.1:g.97017783T>A GRCh37
NC_000007.12:g.96855719T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59824A>T