Canonical Allele Identifier: CA169614013
Gene: DPP6 HGNC NCBI

Linked Data

dbSNP Id: rs761877319
MyVariant Identifiers: chr7:g.153558752T>G (hg19) chr7:g.153861667T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.153861667T>G , CM000669.2:g.153861667T>G GRCh38
NC_000007.13:g.153558752T>G , CM000669.1:g.153558752T>G GRCh37
NC_000007.12:g.153189685T>G NCBI36
NG_033878.2:g.118682T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706130.1:c.60+112659T>G ENSP00000516215.1:n.60+112659T>G
NM_001364497.1:c.60+112659T>G NP_001351426.1:n.60+112659T>G
NM_001364498.1:c.60+112659T>G NP_001351427.1:n.60+112659T>G
NM_001364499.1:c.60+112659T>G NP_001351428.1:n.60+112659T>G
NM_001364500.1:c.60+112659T>G NP_001351429.1:n.60+112659T>G
XR_001745002.1:n.3345+3044T>G
NM_001364497.2:c.60+112659T>G NP_001351426.1:n.60+112659T>G
NM_001364498.2:c.60+112659T>G NP_001351427.1:n.60+112659T>G
NM_001364499.2:c.60+112659T>G NP_001351428.1:n.60+112659T>G
NM_001364500.2:c.60+112659T>G NP_001351429.1:n.60+112659T>G
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