Canonical Allele Identifier: CA129835866

Gene:

Linked Data

• dbSNP Id: rs921599442
• MyVariant Identifiers: chr5:g.158760102A>T (hg19) ; chr5:g.159333094A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159333094A>T , CM000667.2:g.159333094A>T	GRCh38
NC_000005.9:g.158760102A>T , CM000667.1:g.158760102A>T	GRCh37
NC_000005.8:g.158692680A>T	NCBI36
NG_009618.1:g.2380T>A , LRG_71:g.2380T>A

Transcript Alleles

HGVS	Amino-acid change
NR_037889.1:n.745+91A>T