Canonical Allele Identifier: CA806506121

Gene:

Linked Data

• dbSNP Id: rs1243937431
• MyVariant Identifiers: chr5:g.159911463A>T (hg19) ; chr5:g.160484456A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.160484456A>T , CM000667.2:g.160484456A>T	GRCh38
NC_000005.9:g.159911463A>T , CM000667.1:g.159911463A>T	GRCh37
NC_000005.8:g.159844041A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_132748.1:n.191-843A>T