Canonical Allele Identifier: CA3404248

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs748975006
• ExAC: 5:131755563 T / C
• gnomAD v2: 5-131755563-T-C
• MyVariant Identifiers: chr5:g.131755563T>C (hg19) ; chr5:g.132419871T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419871T>C , CM000667.2:g.132419871T>C	GRCh38
NC_000005.9:g.131755563T>C , CM000667.1:g.131755563T>C	GRCh37
NC_000005.8:g.131783462T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-278T>C	ENSP00000492349.2:n.-278T>C
ENST00000638504.1:n.137T>C
ENST00000638568.2:c.-420T>C	ENSP00000491158.2:n.-420T>C
ENST00000639899.1:n.180T>C
ENST00000337752.6:c.-22T>C (CARINH)	ENSP00000338228.2:n.-22T>C
ENST00000378947.7:c.-22T>C (CARINH)	ENSP00000368230.3:n.-22T>C
ENST00000378953.8:c.-22T>C (CARINH)	ENSP00000368236.4:n.-22T>C
ENST00000407797.5:c.-22T>C (CARINH)	ENSP00000385513.1:n.-22T>C
ENST00000461203.5:n.110T>C (CARINH)
ENST00000621237.1:c.-22T>C (CARINH)	ENSP00000481774.1:n.-22T>C
NR_045116.1:n.318T>C (CARINH)
NM_001207001.2:c.-22T>C (CARINH)	NP_001193930.1:n.-22T>C
XR_948788.3:n.894-122A>G (LINC02863)
NR_161242.1:n.162T>C (CARINH)