Canonical Allele Identifier: CA2675201570

Gene: CARINH LINC02863

Linked Data

• gnomAD v4: 5-132419831-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419831A>G , CM000667.2:g.132419831A>G	GRCh38
NC_000005.9:g.131755523A>G , CM000667.1:g.131755523A>G	GRCh37
NC_000005.8:g.131783422A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-318A>G	ENSP00000492349.2:n.-318A>G
ENST00000638504.1:n.97A>G
ENST00000638568.2:c.-460A>G	ENSP00000491158.2:n.-460A>G
ENST00000639899.1:n.140A>G
ENST00000337752.6:c.-62A>G (CARINH)	ENSP00000338228.2:n.-62A>G
ENST00000378947.7:c.-62A>G (CARINH)	ENSP00000368230.3:n.-62A>G
ENST00000378953.8:c.-62A>G (CARINH)	ENSP00000368236.4:n.-62A>G
ENST00000407797.5:c.-62A>G (CARINH)	ENSP00000385513.1:n.-62A>G
ENST00000461203.5:n.70A>G (CARINH)
NR_045116.1:n.278A>G (CARINH)
NM_001207001.2:c.-62A>G (CARINH)	NP_001193930.1:n.-62A>G
XR_948788.3:n.894-82T>C (LINC02863)
NR_161242.1:n.122A>G (CARINH)