Canonical Allele Identifier: CA506044657
Gene: CRLF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18710517A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599707A>C , CM000681.2:g.18599707A>C GRCh38
NC_000019.9:g.18710517A>C , CM000681.1:g.18710517A>C GRCh37
NC_000019.8:g.18571517A>C NCBI36
NG_013370.1:g.12144T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.255T>G ENSP00000506849.1:p.Pro85=
ENST00000392386.8:c.255T>G MANE Select ENSP00000376188.2:p.Pro85=
ENST00000392386.7:c.255T>G ENSP00000376188.2:p.Pro85=
ENST00000593286.1:n.507T>G
NM_004750.4:c.255T>G NP_004741.1:p.Pro85=
XM_011528422.1:c.189T>G XP_011526724.1:p.Pro63=
XM_011528423.1:c.255T>G XP_011526725.1:p.Pro85=
XM_011528424.1:c.189T>G XP_011526726.1:p.Pro63=
XM_011528422.2:c.189T>G XP_011526724.1:p.Pro63=
XM_011528423.2:c.255T>G XP_011526725.1:p.Pro85=
XM_011528424.3:c.189T>G XP_011526726.1:p.Pro63=
NM_004750.5:c.255T>G MANE Select NP_004741.1:p.Pro85=