Canonical Allele Identifier: CA129965531
Gene:

Linked Data

dbSNP Id: rs948998837
gnomAD v3: 5-159581058-T-C
gnomAD v4: 5-159581058-T-C
MyVariant Identifiers: chr5:g.159008065T>C (hg19) chr5:g.159581058T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159581058T>C , CM000667.2:g.159581058T>C GRCh38
NC_000005.9:g.159008065T>C , CM000667.1:g.159008065T>C GRCh37
NC_000005.8:g.158940643T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941139.1:n.2075+623T>C
XR_941140.1:n.2075+623T>C
XR_941141.1:n.570+623T>C
XR_941139.2:n.2229+623T>C
Search 100 bp 5'
Search 100 bp 3'