Canonical Allele Identifier: CA1345065306
Gene: VHL HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10152513G= , CM000665.2:g.10152513G= GRCh38
NC_000003.11:g.10194197G= , CM000665.1:g.10194197G= GRCh37
NC_000003.10:g.10169197G= NCBI36
NG_008212.3:g.15879G= , LRG_322:g.15879G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696153.1:c.*2548G= ENSP00000512444.1:n.*2548G=
ENST00000256474.3:c.*2548G= MANE Select ENSP00000256474.3:n.*2548G=
NM_000551.3:c.*2548G= , LRG_322t1:c.*2548G= NP_000542.1:n.*2548G=
NM_198156.2:c.*2548G= NP_937799.1:n.*2548G=
NM_001354723.1:c.*2744G= NP_001341652.1:n.*2744G=
NM_000551.4:c.*2548G= MANE Select NP_000542.1:n.*2548G=
NM_001354723.2:c.*2744G= NP_001341652.1:n.*2744G=
NM_198156.3:c.*2548G= NP_937799.1:n.*2548G=
Search 100 bp 5'
Search 100 bp 3'