Canonical Allele Identifier: CA3404239

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs376895450
• ExAC: 5:131755534 C / G
• gnomAD v2: 5-131755534-C-G
• gnomAD v3: 5-132419842-C-G
• gnomAD v4: 5-132419842-C-G
• MyVariant Identifiers: chr5:g.131755534C>G (hg19) ; chr5:g.132419842C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419842C>G , CM000667.2:g.132419842C>G	GRCh38
NC_000005.9:g.131755534C>G , CM000667.1:g.131755534C>G	GRCh37
NC_000005.8:g.131783433C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-307C>G	ENSP00000492349.2:n.-307C>G
ENST00000638504.1:n.108C>G
ENST00000638568.2:c.-449C>G	ENSP00000491158.2:n.-449C>G
ENST00000639899.1:n.151C>G
ENST00000337752.6:c.-51C>G (CARINH)	ENSP00000338228.2:n.-51C>G
ENST00000378947.7:c.-51C>G (CARINH)	ENSP00000368230.3:n.-51C>G
ENST00000378953.8:c.-51C>G (CARINH)	ENSP00000368236.4:n.-51C>G
ENST00000407797.5:c.-51C>G (CARINH)	ENSP00000385513.1:n.-51C>G
ENST00000461203.5:n.81C>G (CARINH)
NR_045116.1:n.289C>G (CARINH)
NM_001207001.2:c.-51C>G (CARINH)	NP_001193930.1:n.-51C>G
XR_948788.3:n.894-93G>C (LINC02863)
NR_161242.1:n.133C>G (CARINH)