Canonical Allele Identifier: CA506044598
Gene: CRLF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18710445C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599635C>G , CM000681.2:g.18599635C>G GRCh38
NC_000019.9:g.18710445C>G , CM000681.1:g.18710445C>G GRCh37
NC_000019.8:g.18571445C>G NCBI36
NG_013370.1:g.12216G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.327G>C ENSP00000506849.1:p.Arg109=
ENST00000392386.8:c.327G>C MANE Select ENSP00000376188.2:p.Arg109=
ENST00000392386.7:c.327G>C ENSP00000376188.2:p.Arg109=
NM_004750.4:c.327G>C NP_004741.1:p.Arg109=
XM_011528422.1:c.261G>C XP_011526724.1:p.Arg87=
XM_011528423.1:c.327G>C XP_011526725.1:p.Arg109=
XM_011528424.1:c.261G>C XP_011526726.1:p.Arg87=
XM_011528422.2:c.261G>C XP_011526724.1:p.Arg87=
XM_011528423.2:c.327G>C XP_011526725.1:p.Arg109=
XM_011528424.3:c.261G>C XP_011526726.1:p.Arg87=
NM_004750.5:c.327G>C MANE Select NP_004741.1:p.Arg109=