Canonical Allele Identifier: CA127223790

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs551805284
• gnomAD v3: 5-132419888-A-G
• gnomAD v4: 5-132419888-A-G
• MyVariant Identifiers: chr5:g.131755580A>G (hg19) ; chr5:g.132419888A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419888A>G , CM000667.2:g.132419888A>G	GRCh38
NC_000005.9:g.131755580A>G , CM000667.1:g.131755580A>G	GRCh37
NC_000005.8:g.131783479A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-261A>G	ENSP00000492349.2:n.-261A>G
ENST00000638504.1:n.154A>G
ENST00000638568.2:c.-403A>G	ENSP00000491158.2:n.-403A>G
ENST00000639899.1:n.197A>G
ENST00000337752.6:c.-5A>G (CARINH)	ENSP00000338228.2:n.-5A>G
ENST00000378947.7:c.-5A>G (CARINH)	ENSP00000368230.3:n.-5A>G
ENST00000378953.8:c.-5A>G (CARINH)	ENSP00000368236.4:n.-5A>G
ENST00000407797.5:c.-5A>G (CARINH)	ENSP00000385513.1:n.-5A>G
ENST00000461203.5:n.127A>G (CARINH)
ENST00000621237.1:c.-5A>G (CARINH)	ENSP00000481774.1:n.-5A>G
NR_045116.1:n.335A>G (CARINH)
NM_001207001.2:c.-5A>G (CARINH)	NP_001193930.1:n.-5A>G
XR_948788.3:n.894-139T>C (LINC02863)
NR_161242.1:n.179A>G (CARINH)