Canonical Allele Identifier: CA308901760

Gene: CBLC

Linked Data

• dbSNP Id: rs777117772
• COSMIC: COSM3726897 ; COSM6004253
• MyVariant Identifiers: chr19:g.45296786C>T (hg19) ; chr19:g.44793529C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44793529C>T , CM000681.2:g.44793529C>T	GRCh38
NC_000019.9:g.45296786C>T , CM000681.1:g.45296786C>T	GRCh37
NC_000019.8:g.49988626C>T	NCBI36
NG_054718.1:g.20675C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647358.2:c.1193C>T MANE Select	ENSP00000494162.1:p.Ala398Val
ENST00000270279.7:c.1193C>T	ENSP00000270279.3:p.Ala398Val
ENST00000341505.4:c.1055C>T	ENSP00000340250.4:p.Ala352Val
NM_001130852.1:c.1055C>T	NP_001124324.1:p.Ala352Val
NM_012116.3:c.1193C>T	NP_036248.3:p.Ala398Val
XM_005258696.2:c.1193C>T	XP_005258753.1:p.Ala398Val
XM_011526688.1:c.1193C>T	XP_011524990.1:p.Ala398Val
XM_011526689.1:c.1055C>T	XP_011524991.1:p.Ala352Val
XR_935783.1:n.1140C>T
NM_012116.4:c.1193C>T MANE Select	NP_036248.3:p.Ala398Val
XM_005258696.3:c.1193C>T	XP_005258753.1:p.Ala398Val
XM_011526688.2:c.1193C>T	XP_011524990.1:p.Ala398Val
XM_011526689.2:c.1055C>T	XP_011524991.1:p.Ala352Val
XR_935783.2:n.1145C>T