Canonical Allele Identifier: CA2841849815
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419844C>T , CM000667.2:g.132419844C>T GRCh38
NC_000005.9:g.131755536C>T , CM000667.1:g.131755536C>T GRCh37
NC_000005.8:g.131783435C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-305C>T ENSP00000492349.2:n.-305C>T
ENST00000638504.1:n.110C>T
ENST00000638568.2:c.-447C>T ENSP00000491158.2:n.-447C>T
ENST00000639899.1:n.153C>T
ENST00000337752.6:c.-49C>T (CARINH) ENSP00000338228.2:n.-49C>T
ENST00000378947.7:c.-49C>T (CARINH) ENSP00000368230.3:n.-49C>T
ENST00000378953.8:c.-49C>T (CARINH) ENSP00000368236.4:n.-49C>T
ENST00000407797.5:c.-49C>T (CARINH) ENSP00000385513.1:n.-49C>T
ENST00000461203.5:n.83C>T (CARINH)
NR_045116.1:n.291C>T (CARINH)
NM_001207001.2:c.-49C>T (CARINH) NP_001193930.1:n.-49C>T
XR_948788.3:n.894-95G>A (LINC02863)
NR_161242.1:n.135C>T (CARINH)