Canonical Allele Identifier: CA227359882
Gene: MMP1 HGNC NCBI
WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1018015077
gnomAD v2: 11-102660582-T-A
gnomAD v3: 11-102789851-T-A
gnomAD v4: 11-102789851-T-A
MyVariant Identifiers: chr11:g.102660582T>A (hg19) chr11:g.102789851T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789851T>A , CM000673.2:g.102789851T>A GRCh38
NC_000011.9:g.102660582T>A , CM000673.1:g.102660582T>A GRCh37
NC_000011.8:g.102165792T>A NCBI36
NG_011740.1:g.13385A>T
NG_011740.2:g.13385A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1149A>T (MMP1)
ENST00000681445.1:n.1145A>T (MMP1)
ENST00000681643.1:n.1171A>T (MMP1)
ENST00000371455.7:n.325-8173T>A (WTAPP1)
ENST00000525739.6:n.390-3294T>A (WTAPP1)
ENST00000544704.1:n.344+5787T>A (WTAPP1)
NR_038390.1:n.390-3294T>A (WTAPP1)
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