Canonical Allele Identifier: CA129965387
Gene:

Linked Data

dbSNP Id: rs968732661
MyVariant Identifiers: chr5:g.159007757G>A (hg19) chr5:g.159580749G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580749G>A , CM000667.2:g.159580749G>A GRCh38
NC_000005.9:g.159007757G>A , CM000667.1:g.159007757G>A GRCh37
NC_000005.8:g.158940335G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+314G>A
XR_941140.1:n.2075+314G>A
XR_941141.1:n.570+314G>A
XR_941139.2:n.2229+314G>A
Search 100 bp 5'
Search 100 bp 3'