Canonical Allele Identifier: CA2617231080
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6031393-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6031393G>C , CM000674.2:g.6031393G>C GRCh38
NC_000012.11:g.6140559G>C , CM000674.1:g.6140559G>C GRCh37
NC_000012.10:g.6010820G>C NCBI36
NG_009072.1:g.98278C>G
NG_009072.2:g.98278C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261405.10:c.2820+51C>G MANE Select ENSP00000261405.5:n.2820+51C>G
ENST00000261405.9:c.2820+51C>G ENSP00000261405.5:n.2820+51C>G
ENST00000538635.5:n.421-37459C>G
NM_000552.3:c.2820+51C>G NP_000543.2:n.2820+51C>G
NM_000552.4:c.2820+51C>G NP_000543.2:n.2820+51C>G
NM_000552.5:c.2820+51C>G MANE Select NP_000543.3:n.2820+51C>G
Search 100 bp 5'
Search 100 bp 3'