Canonical Allele Identifier: CA127223903
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Linked Data

dbSNP Id: rs897498248

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132420026T>C , CM000667.2:g.132420026T>C GRCh38
NC_000005.9:g.131755718T>C , CM000667.1:g.131755718T>C GRCh37
NC_000005.8:g.131783617T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638452.2:c.-209+86T>C ENSP00000492349.2:n.-209+86T>C
ENST00000638504.1:n.206+86T>C
ENST00000638568.2:c.-351+86T>C ENSP00000491158.2:n.-351+86T>C
ENST00000639899.1:n.249+86T>C
ENST00000337752.6:c.48+86T>C (CARINH) ENSP00000338228.2:n.48+86T>C
ENST00000378947.7:c.48+86T>C (CARINH) ENSP00000368230.3:n.48+86T>C
ENST00000378953.8:c.48+86T>C (CARINH) ENSP00000368236.4:n.48+86T>C
ENST00000407797.5:c.48+86T>C (CARINH) ENSP00000385513.1:n.48+86T>C
ENST00000461203.5:n.179+86T>C (CARINH)
ENST00000621237.1:c.48+86T>C (CARINH) ENSP00000481774.1:n.48+86T>C
NR_045116.1:n.387+86T>C (CARINH)
NM_001207001.2:c.48+86T>C (CARINH) NP_001193930.1:n.48+86T>C
XR_948788.3:n.894-277A>G (LINC02863)
NR_161242.1:n.231+86T>C (CARINH)