Canonical Allele Identifier: CA360812364

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs1222694265
• gnomAD v2: 5-131755612-A-G
• gnomAD v4: 5-132419920-A-G
• MyVariant Identifiers: chr5:g.131755612A>G (hg19) ; chr5:g.132419920A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419920A>G , CM000667.2:g.132419920A>G	GRCh38
NC_000005.9:g.131755612A>G , CM000667.1:g.131755612A>G	GRCh37
NC_000005.8:g.131783511A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-229A>G	ENSP00000492349.2:n.-229A>G
ENST00000638504.1:n.186A>G
ENST00000638568.2:c.-371A>G	ENSP00000491158.2:n.-371A>G
ENST00000639899.1:n.229A>G
ENST00000337752.6:c.28A>G (CARINH)	ENSP00000338228.2:p.Asn10Asp
ENST00000378947.7:c.28A>G (CARINH)	ENSP00000368230.3:p.Asn10Asp
ENST00000378953.8:c.28A>G (CARINH)	ENSP00000368236.4:p.Asn10Asp
ENST00000407797.5:c.28A>G (CARINH)	ENSP00000385513.1:p.Asn10Asp
ENST00000461203.5:n.159A>G (CARINH)
ENST00000621237.1:c.28A>G (CARINH)	ENSP00000481774.1:p.Asn10Asp
NR_045116.1:n.367A>G (CARINH)
NM_001207001.2:c.28A>G (CARINH)	NP_001193930.1:p.Asn10Asp
XR_948788.3:n.894-171T>C (LINC02863)
NR_161242.1:n.211A>G (CARINH)