Canonical Allele Identifier: CA227359855
Gene: MMP1 HGNC NCBI
WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs777705663
gnomAD v3: 11-102789815-G-A
gnomAD v4: 11-102789815-G-A
MyVariant Identifiers: chr11:g.102660546G>A (hg19) chr11:g.102789815G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789815G>A , CM000673.2:g.102789815G>A GRCh38
NC_000011.9:g.102660546G>A , CM000673.1:g.102660546G>A GRCh37
NC_000011.8:g.102165756G>A NCBI36
NG_011740.1:g.13421C>T
NG_011740.2:g.13421C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1185C>T (MMP1)
ENST00000681445.1:n.1181C>T (MMP1)
ENST00000681643.1:n.1207C>T (MMP1)
ENST00000371455.7:n.325-8209G>A (WTAPP1)
ENST00000525739.6:n.390-3330G>A (WTAPP1)
ENST00000544704.1:n.344+5751G>A (WTAPP1)
NR_038390.1:n.390-3330G>A (WTAPP1)
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