Canonical Allele Identifier: CA1099423685
Gene:

Linked Data

gnomAD v3: 7-24282677-T-A
gnomAD v4: 7-24282677-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24282677T>A , CM000669.2:g.24282677T>A GRCh38
NC_000007.13:g.24322296T>A , CM000669.1:g.24322296T>A GRCh37
NC_000007.12:g.24288821T>A NCBI36
NG_016148.1:g.3490T>A

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-26978A>T XP_016868399.1:n.42-26978A>T
XM_017012911.1:c.42-26978A>T XP_016868400.1:n.42-26978A>T
XR_001745121.1:n.473+36680A>T
XR_001745122.1:n.345-85648A>T
XR_001745123.1:n.473+36680A>T
XR_001745124.1:n.473+36680A>T
XR_001745125.1:n.473+36680A>T
XR_001745126.1:n.473+36680A>T
XR_001745127.1:n.345-26978A>T
XR_001745129.1:n.473+36680A>T
XR_001745130.1:n.473+36680A>T
XR_001745131.1:n.473+36680A>T
XR_001745132.1:n.473+36680A>T