Canonical Allele Identifier: CA351748831
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2931182
ClinVar RCV Id: RCV003782444
dbSNP Id: rs2125124975

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10142047A>C , CM000665.2:g.10142047A>C GRCh38
NC_000003.11:g.10183731A>C , CM000665.1:g.10183731A>C GRCh37
NC_000003.10:g.10158731A>C NCBI36
NG_008212.3:g.5413A>C , LRG_322:g.5413A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696142.1:c.200A>C ENSP00000512434.1:p.Asn67Thr
ENST00000696143.1:c.200A>C ENSP00000512435.1:p.Asn67Thr
ENST00000696153.1:c.200A>C ENSP00000512444.1:p.Asn67Thr
ENST00000256474.3:c.200A>C MANE Select ENSP00000256474.3:p.Asn67Thr
ENST00000256474.2:c.200A>C ENSP00000256474.2:p.Asn67Thr
ENST00000345392.2:c.200A>C ENSP00000344757.2:p.Asn67Thr
NM_000551.3:c.200A>C , LRG_322t1:c.200A>C NP_000542.1:p.Asn67Thr
NM_198156.2:c.200A>C NP_937799.1:p.Asn67Thr
XM_011534078.1:c.200A>C XP_011532380.1:p.Asn67Thr
NM_001354723.1:c.200A>C NP_001341652.1:p.Asn67Thr
NM_000551.4:c.200A>C MANE Select NP_000542.1:p.Asn67Thr
NM_001354723.2:c.200A>C NP_001341652.1:p.Asn67Thr
NM_198156.3:c.200A>C NP_937799.1:p.Asn67Thr