Canonical Allele Identifier: CA2682049079
Gene:

Linked Data

gnomAD v4: 7-24291959-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24291959C>T , CM000669.2:g.24291959C>T GRCh38
NC_000007.13:g.24331578C>T , CM000669.1:g.24331578C>T GRCh37
NC_000007.12:g.24298103C>T NCBI36
NG_016148.1:g.12772C>T

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.41+27398G>A XP_016868399.1:n.41+27398G>A
XM_017012911.1:c.41+27398G>A XP_016868400.1:n.41+27398G>A
XR_001745121.1:n.473+27398G>A
XR_001745122.1:n.345-94930G>A
XR_001745123.1:n.473+27398G>A
XR_001745124.1:n.473+27398G>A
XR_001745125.1:n.473+27398G>A
XR_001745126.1:n.473+27398G>A
XR_001745127.1:n.345-36260G>A
XR_001745129.1:n.473+27398G>A
XR_001745130.1:n.473+27398G>A
XR_001745131.1:n.473+27398G>A
XR_001745132.1:n.473+27398G>A
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