Canonical Allele Identifier: CA9314326
Gene: CRLF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2719035
ClinVar RCV Id: RCV003553441
dbSNP Id: rs7259478
ExAC: 19:18710625 C / T
gnomAD v2: 19-18710625-C-T
gnomAD v3: 19-18599815-C-T
gnomAD v4: 19-18599815-C-T
MyVariant Identifiers: chr19:g.18710625C>T (hg19) chr19:g.18599815C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599815C>T , CM000681.2:g.18599815C>T GRCh38
NC_000019.9:g.18710625C>T , CM000681.1:g.18710625C>T GRCh37
NC_000019.8:g.18571625C>T NCBI36
NG_013370.1:g.12036G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.147G>A ENSP00000506849.1:p.Thr49=
ENST00000392386.8:c.147G>A MANE Select ENSP00000376188.2:p.Thr49=
ENST00000392386.7:c.147G>A ENSP00000376188.2:p.Thr49=
ENST00000593286.1:n.399G>A
NM_004750.4:c.147G>A NP_004741.1:p.Thr49=
XM_011528422.1:c.81G>A XP_011526724.1:p.Thr27=
XM_011528423.1:c.147G>A XP_011526725.1:p.Thr49=
XM_011528424.1:c.81G>A XP_011526726.1:p.Thr27=
XM_011528422.2:c.81G>A XP_011526724.1:p.Thr27=
XM_011528423.2:c.147G>A XP_011526725.1:p.Thr49=
XM_011528424.3:c.81G>A XP_011526726.1:p.Thr27=
NM_004750.5:c.147G>A MANE Select NP_004741.1:p.Thr49=
Search 100 bp 5'
Search 100 bp 3'