Canonical Allele Identifier: CA1345064561

Gene: VHL

Linked Data

• ClinVar Variation Id: 2927689
• ClinVar RCV Id: RCV003784319
• dbSNP Id: rs929301467
• gnomAD v4: 3-10141804-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141804G>A , CM000665.2:g.10141804G>A	GRCh38
NC_000003.11:g.10183488G>A , CM000665.1:g.10183488G>A	GRCh37
NC_000003.10:g.10158488G>A	NCBI36
NG_008212.3:g.5170G>A , LRG_322:g.5170G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.-44G>A	ENSP00000512434.1:n.-44G>A
ENST00000696153.1:c.-44G>A	ENSP00000512444.1:n.-44G>A
ENST00000256474.3:c.-44G>A MANE Select	ENSP00000256474.3:n.-44G>A
ENST00000256474.2:c.-44G>A	ENSP00000256474.2:n.-44G>A
ENST00000345392.2:c.-44G>A	ENSP00000344757.2:n.-44G>A
NM_000551.3:c.-44G>A , LRG_322t1:c.-44G>A	NP_000542.1:n.-44G>A
NM_198156.2:c.-44G>A	NP_937799.1:n.-44G>A
XM_011534078.1:c.-44G>A	XP_011532380.1:n.-44G>A
NM_001354723.1:c.-44G>A	NP_001341652.1:n.-44G>A
NM_000551.4:c.-44G>A MANE Select	NP_000542.1:n.-44G>A
NM_001354723.2:c.-44G>A	NP_001341652.1:n.-44G>A
NM_198156.3:c.-44G>A	NP_937799.1:n.-44G>A