Canonical Allele Identifier: CA232299432
Gene: VWF HGNC NCBI

Linked Data

dbSNP Id: rs767923840
gnomAD v2: 12-6145317-T-C
MyVariant Identifiers: chr12:g.6145317T>C (hg19) chr12:g.6036151T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6036151T>C , CM000674.2:g.6036151T>C GRCh38
NC_000012.11:g.6145317T>C , CM000674.1:g.6145317T>C GRCh37
NC_000012.10:g.6015578T>C NCBI36
NG_009072.1:g.93520A>G
NG_009072.2:g.93520A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261405.10:c.2546+237A>G MANE Select ENSP00000261405.5:n.2546+237A>G
ENST00000261405.9:c.2546+237A>G ENSP00000261405.5:n.2546+237A>G
ENST00000538635.5:n.421-42217A>G
NM_000552.3:c.2546+237A>G NP_000543.2:n.2546+237A>G
NM_000552.4:c.2546+237A>G NP_000543.2:n.2546+237A>G
NM_000552.5:c.2546+237A>G MANE Select NP_000543.3:n.2546+237A>G
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