Canonical Allele Identifier: CA806398720

Gene:

Linked Data

• dbSNP Id: rs1333013656
• gnomAD v3: 5-159333108-C-T
• gnomAD v4: 5-159333108-C-T
• MyVariant Identifiers: chr5:g.158760116C>T (hg19) ; chr5:g.159333108C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159333108C>T , CM000667.2:g.159333108C>T	GRCh38
NC_000005.9:g.158760116C>T , CM000667.1:g.158760116C>T	GRCh37
NC_000005.8:g.158692694C>T	NCBI36
NG_009618.1:g.2366G>A , LRG_71:g.2366G>A

Transcript Alleles

HGVS	Amino-acid change
NR_037889.1:n.745+105C>T