Canonical Allele Identifier: CA506116307
Gene: CRLF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18707472A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18596662A>G , CM000681.2:g.18596662A>G GRCh38
NC_000019.9:g.18707472A>G , CM000681.1:g.18707472A>G GRCh37
NC_000019.8:g.18568472A>G NCBI36
NG_013370.1:g.15189T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.984T>C ENSP00000506849.1:p.Ser328=
ENST00000392386.8:c.984T>C MANE Select ENSP00000376188.2:p.Ser328=
ENST00000392386.7:c.984T>C ENSP00000376188.2:p.Ser328=
ENST00000597131.1:c.447+2T>C
NM_004750.4:c.984T>C NP_004741.1:p.Ser328=
XM_011528422.1:c.918T>C XP_011526724.1:p.Ser306=
XM_011528423.1:c.984T>C XP_011526725.1:p.Ser328=
XM_011528424.1:c.918T>C XP_011526726.1:p.Ser306=
XM_011528422.2:c.918T>C XP_011526724.1:p.Ser306=
XM_011528423.2:c.984T>C XP_011526725.1:p.Ser328=
XM_011528424.3:c.918T>C XP_011526726.1:p.Ser306=
NM_004750.5:c.984T>C MANE Select NP_004741.1:p.Ser328=