Canonical Allele Identifier: CA506044557
Gene: CRLF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18710391G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599581G>C , CM000681.2:g.18599581G>C GRCh38
NC_000019.9:g.18710391G>C , CM000681.1:g.18710391G>C GRCh37
NC_000019.8:g.18571391G>C NCBI36
NG_013370.1:g.12270C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.381C>G ENSP00000506849.1:p.Ser127=
ENST00000392386.8:c.381C>G MANE Select ENSP00000376188.2:p.Ser127=
ENST00000392386.7:c.381C>G ENSP00000376188.2:p.Ser127=
NM_004750.4:c.381C>G NP_004741.1:p.Ser127=
XM_011528422.1:c.315C>G XP_011526724.1:p.Ser105=
XM_011528423.1:c.381C>G XP_011526725.1:p.Ser127=
XM_011528424.1:c.315C>G XP_011526726.1:p.Ser105=
XM_011528422.2:c.315C>G XP_011526724.1:p.Ser105=
XM_011528423.2:c.381C>G XP_011526725.1:p.Ser127=
XM_011528424.3:c.315C>G XP_011526726.1:p.Ser105=
NM_004750.5:c.381C>G MANE Select NP_004741.1:p.Ser127=