Canonical Allele Identifier: CA127223813

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs945907081
• gnomAD v4: 5-132419928-C-T
• MyVariant Identifiers: chr5:g.131755620C>T (hg19) ; chr5:g.132419928C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419928C>T , CM000667.2:g.132419928C>T	GRCh38
NC_000005.9:g.131755620C>T , CM000667.1:g.131755620C>T	GRCh37
NC_000005.8:g.131783519C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-221C>T	ENSP00000492349.2:n.-221C>T
ENST00000638504.1:n.194C>T
ENST00000638568.2:c.-363C>T	ENSP00000491158.2:n.-363C>T
ENST00000639899.1:n.237C>T
ENST00000337752.6:c.36C>T (CARINH)	ENSP00000338228.2:p.Ser12=
ENST00000378947.7:c.36C>T (CARINH)	ENSP00000368230.3:p.Ser12=
ENST00000378953.8:c.36C>T (CARINH)	ENSP00000368236.4:p.Ser12=
ENST00000407797.5:c.36C>T (CARINH)	ENSP00000385513.1:p.Ser12=
ENST00000461203.5:n.167C>T (CARINH)
ENST00000621237.1:c.36C>T (CARINH)	ENSP00000481774.1:p.Ser12=
NR_045116.1:n.375C>T (CARINH)
NM_001207001.2:c.36C>T (CARINH)	NP_001193930.1:p.Ser12=
XR_948788.3:n.894-179G>A (LINC02863)
NR_161242.1:n.219C>T (CARINH)