Canonical Allele Identifier: CA360812320

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs1753236135
• gnomAD v3: 5-132419912-G-T
• gnomAD v4: 5-132419912-G-T
• MyVariant Identifiers: chr5:g.131755604G>T (hg19) ; chr5:g.132419912G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419912G>T , CM000667.2:g.132419912G>T	GRCh38
NC_000005.9:g.131755604G>T , CM000667.1:g.131755604G>T	GRCh37
NC_000005.8:g.131783503G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-237G>T	ENSP00000492349.2:n.-237G>T
ENST00000638504.1:n.178G>T
ENST00000638568.2:c.-379G>T	ENSP00000491158.2:n.-379G>T
ENST00000639899.1:n.221G>T
ENST00000337752.6:c.20G>T (CARINH)	ENSP00000338228.2:p.Gly7Val
ENST00000378947.7:c.20G>T (CARINH)	ENSP00000368230.3:p.Gly7Val
ENST00000378953.8:c.20G>T (CARINH)	ENSP00000368236.4:p.Gly7Val
ENST00000407797.5:c.20G>T (CARINH)	ENSP00000385513.1:p.Gly7Val
ENST00000461203.5:n.151G>T (CARINH)
ENST00000621237.1:c.20G>T (CARINH)	ENSP00000481774.1:p.Gly7Val
NR_045116.1:n.359G>T (CARINH)
NM_001207001.2:c.20G>T (CARINH)	NP_001193930.1:p.Gly7Val
XR_948788.3:n.894-163C>A (LINC02863)
NR_161242.1:n.203G>T (CARINH)