Canonical Allele Identifier: CA342059
Gene: CRLF1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 21428
ClinVar RCV Id: RCV000020613
dbSNP Id: rs104894668

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18594338A>C , CM000681.2:g.18594338A>C GRCh38
NC_000019.9:g.18705148A>C , CM000681.1:g.18705148A>C GRCh37
NC_000019.8:g.18566148A>C NCBI36
NG_013370.1:g.17513T>G

Transcript Alleles

HGVS Amino-acid change
NM_004750.4:c.1121T>G VV NP_004741.1:p.Leu374Arg
XM_011528422.1:c.1055T>G XP_011526724.1:p.Leu352Arg
XM_011528423.1:n.1121T>G XP_011526725.1:p.Leu374Arg
XM_011528424.1:c.1055T>G XP_011526726.1:p.Leu352Arg
XM_011528422.2:c.1055T>G
XM_011528423.2:n.1121T>G
XM_011528424.3:c.1055T>G
NM_004750.5:c.1121T>G VV MANE Preferred
ENST00000392386.7:c.1121T>G ENSP00000376188.2:p.Leu374Arg
ENST00000594325.1:n.98T>G