Canonical Allele Identifier: CA2617231140
Gene: VWF HGNC NCBI

Linked Data

gnomAD v4: 12-6031648-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6031648T>C , CM000674.2:g.6031648T>C GRCh38
NC_000012.11:g.6140814T>C , CM000674.1:g.6140814T>C GRCh37
NC_000012.10:g.6011075T>C NCBI36
NG_009072.1:g.98023A>G
NG_009072.2:g.98023A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2686-70A>G MANE Select ENSP00000261405.5:n.2686-70A>G
ENST00000261405.9:c.2686-70A>G ENSP00000261405.5:n.2686-70A>G
ENST00000538635.5:n.421-37714A>G
NM_000552.3:c.2686-70A>G NP_000543.2:n.2686-70A>G
NM_000552.4:c.2686-70A>G NP_000543.2:n.2686-70A>G
NM_000552.5:c.2686-70A>G MANE Select NP_000543.3:n.2686-70A>G
Search 100 bp 5'
Search 100 bp 3'