Canonical Allele Identifier: CA806398733

Gene:

Linked Data

• dbSNP Id: rs1393949751
• gnomAD v3: 5-159333109-T-G
• gnomAD v4: 5-159333109-T-G
• MyVariant Identifiers: chr5:g.158760117T>G (hg19) ; chr5:g.159333109T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159333109T>G , CM000667.2:g.159333109T>G	GRCh38
NC_000005.9:g.158760117T>G , CM000667.1:g.158760117T>G	GRCh37
NC_000005.8:g.158692695T>G	NCBI36
NG_009618.1:g.2365A>C , LRG_71:g.2365A>C

Transcript Alleles

HGVS	Amino-acid change
NR_037889.1:n.745+106T>G