Canonical Allele Identifier: CA2675201601
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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