Canonical Allele Identifier: CA806430573

Gene:

Linked Data

• dbSNP Id: rs1197190171
• MyVariant Identifiers: chr5:g.159007809A>T (hg19) ; chr5:g.159580801A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159580801A>T , CM000667.2:g.159580801A>T	GRCh38
NC_000005.9:g.159007809A>T , CM000667.1:g.159007809A>T	GRCh37
NC_000005.8:g.158940387A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_941139.1:n.2075+366A>T
XR_941140.1:n.2075+366A>T
XR_941141.1:n.570+366A>T
XR_941139.2:n.2229+366A>T