Canonical Allele Identifier: CA1081638194
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Linked Data

dbSNP Id: rs376824136

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419981C>G , CM000667.2:g.132419981C>G GRCh38
NC_000005.9:g.131755673C>G , CM000667.1:g.131755673C>G GRCh37
NC_000005.8:g.131783572C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638452.2:c.-209+41C>G ENSP00000492349.2:n.-209+41C>G
ENST00000638504.1:n.206+41C>G
ENST00000638568.2:c.-351+41C>G ENSP00000491158.2:n.-351+41C>G
ENST00000639899.1:n.249+41C>G
ENST00000337752.6:c.48+41C>G (CARINH) ENSP00000338228.2:n.48+41C>G
ENST00000378947.7:c.48+41C>G (CARINH) ENSP00000368230.3:n.48+41C>G
ENST00000378953.8:c.48+41C>G (CARINH) ENSP00000368236.4:n.48+41C>G
ENST00000407797.5:c.48+41C>G (CARINH) ENSP00000385513.1:n.48+41C>G
ENST00000461203.5:n.179+41C>G (CARINH)
ENST00000621237.1:c.48+41C>G (CARINH) ENSP00000481774.1:n.48+41C>G
NR_045116.1:n.387+41C>G (CARINH)
NM_001207001.2:c.48+41C>G (CARINH) NP_001193930.1:n.48+41C>G
XR_948788.3:n.894-232G>C (LINC02863)
NR_161242.1:n.231+41C>G (CARINH)