Canonical Allele Identifier: CA129965526
Gene:

Linked Data

dbSNP Id: rs1008171375
MyVariant Identifiers: chr5:g.159008061A>G (hg19) chr5:g.159581054A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159581054A>G , CM000667.2:g.159581054A>G GRCh38
NC_000005.9:g.159008061A>G , CM000667.1:g.159008061A>G GRCh37
NC_000005.8:g.158940639A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941139.1:n.2075+619A>G
XR_941140.1:n.2075+619A>G
XR_941141.1:n.570+619A>G
XR_941139.2:n.2229+619A>G
Search 100 bp 5'
Search 100 bp 3'