Canonical Allele Identifier: CA690489848
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs116684497
MyVariant Identifiers: chr12:g.6140903G>C (hg19) chr12:g.6031737G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6031737G>C , CM000674.2:g.6031737G>C GRCh38
NC_000012.11:g.6140903G>C , CM000674.1:g.6140903G>C GRCh37
NC_000012.10:g.6011164G>C NCBI36
NG_009072.1:g.97934C>G
NG_009072.2:g.97934C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2686-159C>G MANE Select ENSP00000261405.5:n.2686-159C>G
ENST00000261405.9:c.2686-159C>G ENSP00000261405.5:n.2686-159C>G
ENST00000538635.5:n.421-37803C>G
NM_000552.3:c.2686-159C>G NP_000543.2:n.2686-159C>G
NM_000552.4:c.2686-159C>G NP_000543.2:n.2686-159C>G
NM_000552.5:c.2686-159C>G MANE Select NP_000543.3:n.2686-159C>G
Search 100 bp 5'
Search 100 bp 3'