Canonical Allele Identifier: CA2604425120
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419815G>C , CM000667.2:g.132419815G>C GRCh38
NC_000005.9:g.131755507G>C , CM000667.1:g.131755507G>C GRCh37
NC_000005.8:g.131783406G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638452.2:c.-326-8G>C ENSP00000492349.2:n.-326-8G>C
ENST00000638504.1:n.89-8G>C
ENST00000638568.2:c.-468-8G>C ENSP00000491158.2:n.-468-8G>C
ENST00000639899.1:n.132-8G>C
ENST00000337752.6:c.-70-8G>C (CARINH) ENSP00000338228.2:n.-70-8G>C
ENST00000378947.7:c.-70-8G>C (CARINH) ENSP00000368230.3:n.-70-8G>C
ENST00000378953.8:c.-70-8G>C (CARINH) ENSP00000368236.4:n.-70-8G>C
ENST00000407797.5:c.-70-8G>C (CARINH) ENSP00000385513.1:n.-70-8G>C
ENST00000461203.5:n.62-8G>C (CARINH)
NR_045116.1:n.270-8G>C (CARINH)
NM_001207001.2:c.-70-8G>C (CARINH) NP_001193930.1:n.-70-8G>C
XR_948788.3:n.894-66C>G (LINC02863)
NR_161242.1:n.114-8G>C (CARINH)