Canonical Allele Identifier: CA506044594
Gene: CRLF1 HGNC NCBI

Linked Data

dbSNP Id: rs1301659724

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599632C>A , CM000681.2:g.18599632C>A GRCh38
NC_000019.9:g.18710442C>A , CM000681.1:g.18710442C>A GRCh37
NC_000019.8:g.18571442C>A NCBI36
NG_013370.1:g.12219G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.330G>T ENSP00000506849.1:p.Ser110=
ENST00000392386.8:c.330G>T MANE Select ENSP00000376188.2:p.Ser110=
ENST00000392386.7:c.330G>T ENSP00000376188.2:p.Ser110=
NM_004750.4:c.330G>T NP_004741.1:p.Ser110=
XM_011528422.1:c.264G>T XP_011526724.1:p.Ser88=
XM_011528423.1:c.330G>T XP_011526725.1:p.Ser110=
XM_011528424.1:c.264G>T XP_011526726.1:p.Ser88=
XM_011528422.2:c.264G>T XP_011526724.1:p.Ser88=
XM_011528423.2:c.330G>T XP_011526725.1:p.Ser110=
XM_011528424.3:c.264G>T XP_011526726.1:p.Ser88=
NM_004750.5:c.330G>T MANE Select NP_004741.1:p.Ser110=