Canonical Allele Identifier: CA039977
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs758034030
gnomAD v2: 3-10183774-G-A
gnomAD v4: 3-10142090-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142090G>A , CM000665.2:g.10142090G>A GRCh38
NC_000003.11:g.10183774G>A , CM000665.1:g.10183774G>A GRCh37
NC_000003.10:g.10158774G>A NCBI36
NG_008212.3:g.5456G>A , LRG_322:g.5456G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.243G>A ENSP00000512434.1:p.Pro81=
ENST00000696143.1:c.243G>A ENSP00000512435.1:p.Pro81=
ENST00000696153.1:c.243G>A ENSP00000512444.1:p.Pro81=
ENST00000256474.3:c.243G>A MANE Select ENSP00000256474.3:p.Pro81=
ENST00000256474.2:c.243G>A ENSP00000256474.2:p.Pro81=
ENST00000345392.2:c.243G>A ENSP00000344757.2:p.Pro81=
NM_000551.3:c.243G>A , LRG_322t1:c.243G>A NP_000542.1:p.Pro81=
NM_198156.2:c.243G>A NP_937799.1:p.Pro81=
XM_011534078.1:c.243G>A XP_011532380.1:p.Pro81=
NM_001354723.1:c.243G>A NP_001341652.1:p.Pro81=
NM_000551.4:c.243G>A MANE Select NP_000542.1:p.Pro81=
NM_001354723.2:c.243G>A NP_001341652.1:p.Pro81=
NM_198156.3:c.243G>A NP_937799.1:p.Pro81=