Canonical Allele Identifier: CA803778373

Gene:

Linked Data

• dbSNP Id: rs1476100887
• MyVariant Identifiers: chr5:g.128722534T>G (hg19) ; chr5:g.129386841T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.129386841T>G , CM000667.2:g.129386841T>G	GRCh38
NC_000005.9:g.128722534T>G , CM000667.1:g.128722534T>G	GRCh37
NC_000005.8:g.128750433T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_427770.2:n.163-1607T>G
XR_948774.1:n.235-5810T>G
XR_001742463.1:n.4089-1607T>G
XR_001742464.1:n.2019-5810T>G
XR_001742465.1:n.401-1607T>G
XR_427770.3:n.337-1607T>G