Canonical Allele Identifier: CA670869843
Gene: MMP1 HGNC NCBI
WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1341655463
gnomAD v3: 11-102789794-G-T
gnomAD v4: 11-102789794-G-T
MyVariant Identifiers: chr11:g.102660525G>T (hg19) chr11:g.102789794G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789794G>T , CM000673.2:g.102789794G>T GRCh38
NC_000011.9:g.102660525G>T , CM000673.1:g.102660525G>T GRCh37
NC_000011.8:g.102165735G>T NCBI36
NG_011740.1:g.13442C>A
NG_011740.2:g.13442C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1206C>A (MMP1)
ENST00000681445.1:n.1202C>A (MMP1)
ENST00000681643.1:n.1228C>A (MMP1)
ENST00000371455.7:n.325-8230G>T (WTAPP1)
ENST00000525739.6:n.390-3351G>T (WTAPP1)
ENST00000544704.1:n.344+5730G>T (WTAPP1)
NR_038390.1:n.390-3351G>T (WTAPP1)
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