Canonical Allele Identifier: CA2675201576
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419840G>T , CM000667.2:g.132419840G>T GRCh38
NC_000005.9:g.131755532G>T , CM000667.1:g.131755532G>T GRCh37
NC_000005.8:g.131783431G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-309G>T ENSP00000492349.2:n.-309G>T
ENST00000638504.1:n.106G>T
ENST00000638568.2:c.-451G>T ENSP00000491158.2:n.-451G>T
ENST00000639899.1:n.149G>T
ENST00000337752.6:c.-53G>T (CARINH) ENSP00000338228.2:n.-53G>T
ENST00000378947.7:c.-53G>T (CARINH) ENSP00000368230.3:n.-53G>T
ENST00000378953.8:c.-53G>T (CARINH) ENSP00000368236.4:n.-53G>T
ENST00000407797.5:c.-53G>T (CARINH) ENSP00000385513.1:n.-53G>T
ENST00000461203.5:n.79G>T (CARINH)
NR_045116.1:n.287G>T (CARINH)
NM_001207001.2:c.-53G>T (CARINH) NP_001193930.1:n.-53G>T
XR_948788.3:n.894-91C>A (LINC02863)
NR_161242.1:n.131G>T (CARINH)