Canonical Allele Identifier: CA127224004

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs918897027
• gnomAD v3: 5-132420392-C-G
• gnomAD v4: 5-132420392-C-G
• MyVariant Identifiers: chr5:g.132420392C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132420392C>G , CM000667.2:g.132420392C>G	GRCh38
NC_000005.9:g.131756084C>G , CM000667.1:g.131756084C>G	GRCh37
NC_000005.8:g.131783983C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-209+452C>G	ENSP00000492349.2:n.-209+452C>G
ENST00000638504.1:n.206+452C>G
ENST00000638568.2:c.-351+452C>G	ENSP00000491158.2:n.-351+452C>G
ENST00000639899.1:n.249+452C>G
ENST00000337752.6:c.48+452C>G (CARINH)	ENSP00000338228.2:n.48+452C>G
ENST00000378947.7:c.48+452C>G (CARINH)	ENSP00000368230.3:n.48+452C>G
ENST00000378953.8:c.48+452C>G (CARINH)	ENSP00000368236.4:n.48+452C>G
ENST00000407797.5:c.48+452C>G (CARINH)	ENSP00000385513.1:n.48+452C>G
ENST00000461203.5:n.179+452C>G (CARINH)
ENST00000621237.1:c.48+452C>G (CARINH)	ENSP00000481774.1:n.48+452C>G
NR_045116.1:n.387+452C>G (CARINH)
NM_001207001.2:c.48+452C>G (CARINH)	NP_001193930.1:n.48+452C>G
XR_948788.3:n.894-643G>C (LINC02863)
NR_161242.1:n.231+452C>G (CARINH)