Canonical Allele Identifier: CA127223514

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs565865193
• gnomAD v3: 5-132419469-G-T
• gnomAD v4: 5-132419469-G-T
• MyVariant Identifiers: chr5:g.131755161G>T (hg19) ; chr5:g.132419469G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419469G>T , CM000667.2:g.132419469G>T	GRCh38
NC_000005.9:g.131755161G>T , CM000667.1:g.131755161G>T	GRCh37
NC_000005.8:g.131783060G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-326-354G>T	ENSP00000492349.2:n.-326-354G>T
ENST00000638504.1:n.89-354G>T
ENST00000638568.2:c.-468-354G>T	ENSP00000491158.2:n.-468-354G>T
ENST00000639899.1:n.132-354G>T
ENST00000337752.6:c.-70-354G>T (CARINH)	ENSP00000338228.2:n.-70-354G>T
ENST00000378947.7:c.-70-354G>T (CARINH)	ENSP00000368230.3:n.-70-354G>T
ENST00000378953.8:c.-70-354G>T (CARINH)	ENSP00000368236.4:n.-70-354G>T
ENST00000407797.5:c.-70-354G>T (CARINH)	ENSP00000385513.1:n.-70-354G>T
ENST00000461203.5:n.62-354G>T (CARINH)
NR_045116.1:n.270-354G>T (CARINH)
NM_001207001.2:c.-70-354G>T (CARINH)	NP_001193930.1:n.-70-354G>T
XR_948788.3:n.1174C>A (LINC02863)
NR_161242.1:n.114-354G>T (CARINH)