Canonical Allele Identifier: CA342060
Gene: CRLF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39410
dbSNP Id: rs104894670

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599720C>T , CM000681.2:g.18599720C>T GRCh38
NC_000019.9:g.18710530C>T , CM000681.1:g.18710530C>T GRCh37
NC_000019.8:g.18571530C>T NCBI36
NG_013370.1:g.12131G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.242G>A ENSP00000506849.1:p.Arg81His
ENST00000392386.8:c.242G>A MANE Select ENSP00000376188.2:p.Arg81His
ENST00000392386.7:c.242G>A ENSP00000376188.2:p.Arg81His
ENST00000593286.1:n.494G>A
NM_004750.4:c.242G>A NP_004741.1:p.Arg81His
XM_011528422.1:c.176G>A XP_011526724.1:p.Arg59His
XM_011528423.1:c.242G>A XP_011526725.1:p.Arg81His
XM_011528424.1:c.176G>A XP_011526726.1:p.Arg59His
XM_011528422.2:c.176G>A XP_011526724.1:p.Arg59His
XM_011528423.2:c.242G>A XP_011526725.1:p.Arg81His
XM_011528424.3:c.176G>A XP_011526726.1:p.Arg59His
NM_004750.5:c.242G>A MANE Select NP_004741.1:p.Arg81His