Canonical Allele Identifier: CA563057222

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs1477332777
• gnomAD v2: 5-131755536-C-A
• gnomAD v3: 5-132419844-C-A
• gnomAD v4: 5-132419844-C-A
• MyVariant Identifiers: chr5:g.131755536C>A (hg19) ; chr5:g.132419844C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419844C>A , CM000667.2:g.132419844C>A	GRCh38
NC_000005.9:g.131755536C>A , CM000667.1:g.131755536C>A	GRCh37
NC_000005.8:g.131783435C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-305C>A	ENSP00000492349.2:n.-305C>A
ENST00000638504.1:n.110C>A
ENST00000638568.2:c.-447C>A	ENSP00000491158.2:n.-447C>A
ENST00000639899.1:n.153C>A
ENST00000337752.6:c.-49C>A (CARINH)	ENSP00000338228.2:n.-49C>A
ENST00000378947.7:c.-49C>A (CARINH)	ENSP00000368230.3:n.-49C>A
ENST00000378953.8:c.-49C>A (CARINH)	ENSP00000368236.4:n.-49C>A
ENST00000407797.5:c.-49C>A (CARINH)	ENSP00000385513.1:n.-49C>A
ENST00000461203.5:n.83C>A (CARINH)
NR_045116.1:n.291C>A (CARINH)
NM_001207001.2:c.-49C>A (CARINH)	NP_001193930.1:n.-49C>A
XR_948788.3:n.894-95G>T (LINC02863)
NR_161242.1:n.135C>A (CARINH)