Canonical Allele Identifier: CA9314285
Gene: CRLF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 738541
ClinVar RCV Id: RCV000914438
dbSNP Id: rs117193413
ExAC: 19:18710461 T / C
gnomAD v2: 19-18710461-T-C
gnomAD v3: 19-18599651-T-C
gnomAD v4: 19-18599651-T-C
MyVariant Identifiers: chr19:g.18710461T>C (hg19) chr19:g.18599651T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599651T>C , CM000681.2:g.18599651T>C GRCh38
NC_000019.9:g.18710461T>C , CM000681.1:g.18710461T>C GRCh37
NC_000019.8:g.18571461T>C NCBI36
NG_013370.1:g.12200A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.311A>G ENSP00000506849.1:p.Asn104Ser
ENST00000392386.8:c.311A>G MANE Select ENSP00000376188.2:p.Asn104Ser
ENST00000392386.7:c.311A>G ENSP00000376188.2:p.Asn104Ser
NM_004750.4:c.311A>G NP_004741.1:p.Asn104Ser
XM_011528422.1:c.245A>G XP_011526724.1:p.Asn82Ser
XM_011528423.1:c.311A>G XP_011526725.1:p.Asn104Ser
XM_011528424.1:c.245A>G XP_011526726.1:p.Asn82Ser
XM_011528422.2:c.245A>G XP_011526724.1:p.Asn82Ser
XM_011528423.2:c.311A>G XP_011526725.1:p.Asn104Ser
XM_011528424.3:c.245A>G XP_011526726.1:p.Asn82Ser
NM_004750.5:c.311A>G MANE Select NP_004741.1:p.Asn104Ser
Search 100 bp 5'
Search 100 bp 3'