Canonical Allele Identifier: CA2984463962
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419863C>T , CM000667.2:g.132419863C>T GRCh38
NC_000005.9:g.131755555C>T , CM000667.1:g.131755555C>T GRCh37
NC_000005.8:g.131783454C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-286C>T ENSP00000492349.2:n.-286C>T
ENST00000638504.1:n.129C>T
ENST00000638568.2:c.-428C>T ENSP00000491158.2:n.-428C>T
ENST00000639899.1:n.172C>T
ENST00000337752.6:c.-30C>T (CARINH) ENSP00000338228.2:n.-30C>T
ENST00000378947.7:c.-30C>T (CARINH) ENSP00000368230.3:n.-30C>T
ENST00000378953.8:c.-30C>T (CARINH) ENSP00000368236.4:n.-30C>T
ENST00000407797.5:c.-30C>T (CARINH) ENSP00000385513.1:n.-30C>T
ENST00000461203.5:n.102C>T (CARINH)
NR_045116.1:n.310C>T (CARINH)
NM_001207001.2:c.-30C>T (CARINH) NP_001193930.1:n.-30C>T
XR_948788.3:n.894-114G>A (LINC02863)
NR_161242.1:n.154C>T (CARINH)