Canonical Allele Identifier: CA404852088
Gene: CRLF1 HGNC NCBI

Linked Data

dbSNP Id: rs1204287865

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599712G>A , CM000681.2:g.18599712G>A GRCh38
NC_000019.9:g.18710522G>A , CM000681.1:g.18710522G>A GRCh37
NC_000019.8:g.18571522G>A NCBI36
NG_013370.1:g.12139C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.250C>T ENSP00000506849.1:p.Pro84Ser
ENST00000392386.8:c.250C>T MANE Select ENSP00000376188.2:p.Pro84Ser
ENST00000392386.7:c.250C>T ENSP00000376188.2:p.Pro84Ser
ENST00000593286.1:n.502C>T
NM_004750.4:c.250C>T NP_004741.1:p.Pro84Ser
XM_011528422.1:c.184C>T XP_011526724.1:p.Pro62Ser
XM_011528423.1:c.250C>T XP_011526725.1:p.Pro84Ser
XM_011528424.1:c.184C>T XP_011526726.1:p.Pro62Ser
XM_011528422.2:c.184C>T XP_011526724.1:p.Pro62Ser
XM_011528423.2:c.250C>T XP_011526725.1:p.Pro84Ser
XM_011528424.3:c.184C>T XP_011526726.1:p.Pro62Ser
NM_004750.5:c.250C>T MANE Select NP_004741.1:p.Pro84Ser