Canonical Allele Identifier: CA2675201581
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419848C>T , CM000667.2:g.132419848C>T GRCh38
NC_000005.9:g.131755540C>T , CM000667.1:g.131755540C>T GRCh37
NC_000005.8:g.131783439C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-301C>T ENSP00000492349.2:n.-301C>T
ENST00000638504.1:n.114C>T
ENST00000638568.2:c.-443C>T ENSP00000491158.2:n.-443C>T
ENST00000639899.1:n.157C>T
ENST00000337752.6:c.-45C>T (CARINH) ENSP00000338228.2:n.-45C>T
ENST00000378947.7:c.-45C>T (CARINH) ENSP00000368230.3:n.-45C>T
ENST00000378953.8:c.-45C>T (CARINH) ENSP00000368236.4:n.-45C>T
ENST00000407797.5:c.-45C>T (CARINH) ENSP00000385513.1:n.-45C>T
ENST00000461203.5:n.87C>T (CARINH)
NR_045116.1:n.295C>T (CARINH)
NM_001207001.2:c.-45C>T (CARINH) NP_001193930.1:n.-45C>T
XR_948788.3:n.894-99G>A (LINC02863)
NR_161242.1:n.139C>T (CARINH)