Canonical Allele Identifier: CA383495166

Gene: VWF

Linked Data

• gnomAD v4: 12-6016137-C-A
• MyVariant Identifiers: chr12:g.6125303C>A (hg19) ; chr12:g.6016137C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6016137C>A , CM000674.2:g.6016137C>A	GRCh38
NC_000012.11:g.6125303C>A , CM000674.1:g.6125303C>A	GRCh37
NC_000012.10:g.5995564C>A	NCBI36
NG_009072.1:g.113534G>T
NG_009072.2:g.113534G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261405.10:c.5407G>T MANE Select	ENSP00000261405.5:p.Val1803Phe
ENST00000261405.9:c.5407G>T	ENSP00000261405.5:p.Val1803Phe
ENST00000538635.5:n.421-22203G>T
NM_000552.3:c.5407G>T	NP_000543.2:p.Val1803Phe
NM_000552.4:c.5407G>T	NP_000543.2:p.Val1803Phe
NM_000552.5:c.5407G>T MANE Select	NP_000543.3:p.Val1803Phe