Canonical Allele Identifier: CA2675201542
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Linked Data

gnomAD v4: 5-132419807-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419807C>A , CM000667.2:g.132419807C>A GRCh38
NC_000005.9:g.131755499C>A , CM000667.1:g.131755499C>A GRCh37
NC_000005.8:g.131783398C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638452.2:c.-326-16C>A ENSP00000492349.2:n.-326-16C>A
ENST00000638504.1:n.89-16C>A
ENST00000638568.2:c.-468-16C>A ENSP00000491158.2:n.-468-16C>A
ENST00000639899.1:n.132-16C>A
ENST00000337752.6:c.-70-16C>A (CARINH) ENSP00000338228.2:n.-70-16C>A
ENST00000378947.7:c.-70-16C>A (CARINH) ENSP00000368230.3:n.-70-16C>A
ENST00000378953.8:c.-70-16C>A (CARINH) ENSP00000368236.4:n.-70-16C>A
ENST00000407797.5:c.-70-16C>A (CARINH) ENSP00000385513.1:n.-70-16C>A
ENST00000461203.5:n.62-16C>A (CARINH)
NR_045116.1:n.270-16C>A (CARINH)
NM_001207001.2:c.-70-16C>A (CARINH) NP_001193930.1:n.-70-16C>A
XR_948788.3:n.894-58G>T (LINC02863)
NR_161242.1:n.114-16C>A (CARINH)
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