Canonical Allele Identifier: CA1583158603

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs1580906683

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419847A>C , CM000667.2:g.132419847A>C	GRCh38
NC_000005.9:g.131755539A>C , CM000667.1:g.131755539A>C	GRCh37
NC_000005.8:g.131783438A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-302A>C	ENSP00000492349.2:n.-302A>C
ENST00000638504.1:n.113A>C
ENST00000638568.2:c.-444A>C	ENSP00000491158.2:n.-444A>C
ENST00000639899.1:n.156A>C
ENST00000337752.6:c.-46A>C (CARINH)	ENSP00000338228.2:n.-46A>C
ENST00000378947.7:c.-46A>C (CARINH)	ENSP00000368230.3:n.-46A>C
ENST00000378953.8:c.-46A>C (CARINH)	ENSP00000368236.4:n.-46A>C
ENST00000407797.5:c.-46A>C (CARINH)	ENSP00000385513.1:n.-46A>C
ENST00000461203.5:n.86A>C (CARINH)
NR_045116.1:n.294A>C (CARINH)
NM_001207001.2:c.-46A>C (CARINH)	NP_001193930.1:n.-46A>C
XR_948788.3:n.894-98T>G (LINC02863)
NR_161242.1:n.138A>C (CARINH)