Canonical Allele Identifier: CA432536163

Gene: VHL

Linked Data

• ClinVar Variation Id: 1736844
• ClinVar RCV Id: RCV002321159
• dbSNP Id: rs996469746
• MyVariant Identifiers: chr3:g.10183570A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141886A>C , CM000665.2:g.10141886A>C	GRCh38
NC_000003.11:g.10183570A>C , CM000665.1:g.10183570A>C	GRCh37
NC_000003.10:g.10158570A>C	NCBI36
NG_008212.3:g.5252A>C , LRG_322:g.5252A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.39A>C	ENSP00000512434.1:p.Val13=
ENST00000696143.1:c.39A>C	ENSP00000512435.1:p.Val13=
ENST00000696153.1:c.39A>C	ENSP00000512444.1:p.Val13=
ENST00000256474.3:c.39A>C MANE Select	ENSP00000256474.3:p.Val13=
ENST00000256474.2:c.39A>C	ENSP00000256474.2:p.Val13=
ENST00000345392.2:c.39A>C	ENSP00000344757.2:p.Val13=
NM_000551.3:c.39A>C , LRG_322t1:c.39A>C	NP_000542.1:p.Val13=
NM_198156.2:c.39A>C	NP_937799.1:p.Val13=
XM_011534078.1:c.39A>C	XP_011532380.1:p.Val13=
NM_001354723.1:c.39A>C	NP_001341652.1:p.Val13=
NM_000551.4:c.39A>C MANE Select	NP_000542.1:p.Val13=
NM_001354723.2:c.39A>C	NP_001341652.1:p.Val13=
NM_198156.3:c.39A>C	NP_937799.1:p.Val13=