Canonical Allele Identifier: CA893994476
Gene: VAMP5 HGNC NCBI

Linked Data

dbSNP Id: rs987107553
MyVariant Identifiers: chr2:g.85816399C>G (hg19) chr2:g.85589276C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85589276C>G , CM000664.2:g.85589276C>G GRCh38
NC_000002.11:g.85816399C>G , CM000664.1:g.85816399C>G GRCh37
NC_000002.10:g.85669910C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306384.5:c.4-2449C>G MANE Select ENSP00000305647.4:n.4-2449C>G
ENST00000306384.4:c.4-2449C>G ENSP00000305647.4:n.4-2449C>G
NM_006634.2:c.4-2449C>G NP_006625.1:n.4-2449C>G
NM_006634.3:c.4-2449C>G MANE Select NP_006625.1:n.4-2449C>G
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