Canonical Allele Identifier: CA9314296

Gene: CRLF1

Linked Data

• dbSNP Id: rs774598847
• ExAC: 19:18710514 C / T
• gnomAD v2: 19-18710514-C-T
• gnomAD v4: 19-18599704-C-T
• MyVariant Identifiers: chr19:g.18710514C>T (hg19) ; chr19:g.18599704C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18599704C>T , CM000681.2:g.18599704C>T	GRCh38
NC_000019.9:g.18710514C>T , CM000681.1:g.18710514C>T	GRCh37
NC_000019.8:g.18571514C>T	NCBI36
NG_013370.1:g.12147G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.258G>A	ENSP00000506849.1:p.Glu86=
ENST00000392386.8:c.258G>A MANE Select	ENSP00000376188.2:p.Glu86=
ENST00000392386.7:c.258G>A	ENSP00000376188.2:p.Glu86=
ENST00000593286.1:n.510G>A
NM_004750.4:c.258G>A	NP_004741.1:p.Glu86=
XM_011528422.1:c.192G>A	XP_011526724.1:p.Glu64=
XM_011528423.1:c.258G>A	XP_011526725.1:p.Glu86=
XM_011528424.1:c.192G>A	XP_011526726.1:p.Glu64=
XM_011528422.2:c.192G>A	XP_011526724.1:p.Glu64=
XM_011528423.2:c.258G>A	XP_011526725.1:p.Glu86=
XM_011528424.3:c.192G>A	XP_011526726.1:p.Glu64=
NM_004750.5:c.258G>A MANE Select	NP_004741.1:p.Glu86=