Canonical Allele Identifier: CA506044610
Gene: CRLF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18710463G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18599653G>A , CM000681.2:g.18599653G>A GRCh38
NC_000019.9:g.18710463G>A , CM000681.1:g.18710463G>A GRCh37
NC_000019.8:g.18571463G>A NCBI36
NG_013370.1:g.12198C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684169.1:c.309C>T ENSP00000506849.1:p.Leu103=
ENST00000392386.8:c.309C>T MANE Select ENSP00000376188.2:p.Leu103=
ENST00000392386.7:c.309C>T ENSP00000376188.2:p.Leu103=
NM_004750.4:c.309C>T NP_004741.1:p.Leu103=
XM_011528422.1:c.243C>T XP_011526724.1:p.Leu81=
XM_011528423.1:c.309C>T XP_011526725.1:p.Leu103=
XM_011528424.1:c.243C>T XP_011526726.1:p.Leu81=
XM_011528422.2:c.243C>T XP_011526724.1:p.Leu81=
XM_011528423.2:c.309C>T XP_011526725.1:p.Leu103=
XM_011528424.3:c.243C>T XP_011526726.1:p.Leu81=
NM_004750.5:c.309C>T MANE Select NP_004741.1:p.Leu103=