Canonical Allele Identifier: CA360812357

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs1361129515
• gnomAD v2: 5-131755611-G-T
• MyVariant Identifiers: chr5:g.131755611G>T (hg19) ; chr5:g.132419919G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132419919G>T , CM000667.2:g.132419919G>T	GRCh38
NC_000005.9:g.131755611G>T , CM000667.1:g.131755611G>T	GRCh37
NC_000005.8:g.131783510G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000638452.2:c.-230G>T	ENSP00000492349.2:n.-230G>T
ENST00000638504.1:n.185G>T
ENST00000638568.2:c.-372G>T	ENSP00000491158.2:n.-372G>T
ENST00000639899.1:n.228G>T
ENST00000337752.6:c.27G>T (CARINH)	ENSP00000338228.2:p.Leu9Phe
ENST00000378947.7:c.27G>T (CARINH)	ENSP00000368230.3:p.Leu9Phe
ENST00000378953.8:c.27G>T (CARINH)	ENSP00000368236.4:p.Leu9Phe
ENST00000407797.5:c.27G>T (CARINH)	ENSP00000385513.1:p.Leu9Phe
ENST00000461203.5:n.158G>T (CARINH)
ENST00000621237.1:c.27G>T (CARINH)	ENSP00000481774.1:p.Leu9Phe
NR_045116.1:n.366G>T (CARINH)
NM_001207001.2:c.27G>T (CARINH)	NP_001193930.1:p.Leu9Phe
XR_948788.3:n.894-170C>A (LINC02863)
NR_161242.1:n.210G>T (CARINH)