Canonical Allele Identifier: CA3404245

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs376087038
• ExAC: 5:131755545 C / T
• gnomAD v2: 5-131755545-C-T
• gnomAD v3: 5-132419853-C-T
• gnomAD v4: 5-132419853-C-T
• MyVariant Identifiers: chr5:g.131755545C>T (hg19) ; chr5:g.132419853C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419853C>T , CM000667.2:g.132419853C>T	GRCh38
NC_000005.9:g.131755545C>T , CM000667.1:g.131755545C>T	GRCh37
NC_000005.8:g.131783444C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-296C>T	ENSP00000492349.2:n.-296C>T
ENST00000638504.1:n.119C>T
ENST00000638568.2:c.-438C>T	ENSP00000491158.2:n.-438C>T
ENST00000639899.1:n.162C>T
ENST00000337752.6:c.-40C>T (CARINH)	ENSP00000338228.2:n.-40C>T
ENST00000378947.7:c.-40C>T (CARINH)	ENSP00000368230.3:n.-40C>T
ENST00000378953.8:c.-40C>T (CARINH)	ENSP00000368236.4:n.-40C>T
ENST00000407797.5:c.-40C>T (CARINH)	ENSP00000385513.1:n.-40C>T
ENST00000461203.5:n.92C>T (CARINH)
NR_045116.1:n.300C>T (CARINH)
NM_001207001.2:c.-40C>T (CARINH)	NP_001193930.1:n.-40C>T
XR_948788.3:n.894-104G>A (LINC02863)
NR_161242.1:n.144C>T (CARINH)