Canonical Allele Identifier: CA227367872
Gene: WTAPP1 HGNC NCBI
MMP1 HGNC NCBI

Linked Data

dbSNP Id: rs1015706782
gnomAD v3: 11-102798187-T-C
gnomAD v4: 11-102798187-T-C
MyVariant Identifiers: chr11:g.102668918T>C (hg19) chr11:g.102798187T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798187T>C , CM000673.2:g.102798187T>C GRCh38
NC_000011.9:g.102668918T>C , CM000673.1:g.102668918T>C GRCh37
NC_000011.8:g.102174128T>C NCBI36
NG_011740.1:g.5049A>G
NG_011740.2:g.5049A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+65T>C (WTAPP1)
ENST00000525739.6:n.682+65T>C (WTAPP1)
ENST00000544704.1:n.443+65T>C (WTAPP1)
NM_001145938.1:c.-141A>G (MMP1) NP_001139410.1:n.-141A>G
NM_002421.3:c.-95A>G (MMP1) NP_002412.1:n.-95A>G
NR_038390.1:n.682+65T>C (WTAPP1)
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