Canonical Allele Identifier: CA2675201605
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419867A>G , CM000667.2:g.132419867A>G GRCh38
NC_000005.9:g.131755559A>G , CM000667.1:g.131755559A>G GRCh37
NC_000005.8:g.131783458A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638452.2:c.-282A>G ENSP00000492349.2:n.-282A>G
ENST00000638504.1:n.133A>G
ENST00000638568.2:c.-424A>G ENSP00000491158.2:n.-424A>G
ENST00000639899.1:n.176A>G
ENST00000337752.6:c.-26A>G (CARINH) ENSP00000338228.2:n.-26A>G
ENST00000378947.7:c.-26A>G (CARINH) ENSP00000368230.3:n.-26A>G
ENST00000378953.8:c.-26A>G (CARINH) ENSP00000368236.4:n.-26A>G
ENST00000407797.5:c.-26A>G (CARINH) ENSP00000385513.1:n.-26A>G
ENST00000461203.5:n.106A>G (CARINH)
ENST00000621237.1:c.-26A>G (CARINH) ENSP00000481774.1:n.-26A>G
NR_045116.1:n.314A>G (CARINH)
NM_001207001.2:c.-26A>G (CARINH) NP_001193930.1:n.-26A>G
XR_948788.3:n.894-118T>C (LINC02863)
NR_161242.1:n.158A>G (CARINH)