Canonical Allele Identifier: CA227359701
Gene: MMP1 HGNC NCBI
WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs759917854
MyVariant Identifiers: chr11:g.102660394C>T (hg19) chr11:g.102789663C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789663C>T , CM000673.2:g.102789663C>T GRCh38
NC_000011.9:g.102660394C>T , CM000673.1:g.102660394C>T GRCh37
NC_000011.8:g.102165604C>T NCBI36
NG_011740.1:g.13573G>A
NG_011740.2:g.13573G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1337G>A (MMP1)
ENST00000681445.1:n.1333G>A (MMP1)
ENST00000681643.1:n.1359G>A (MMP1)
ENST00000371455.7:n.325-8361C>T (WTAPP1)
ENST00000525739.6:n.390-3482C>T (WTAPP1)
ENST00000544704.1:n.344+5599C>T (WTAPP1)
NR_038390.1:n.390-3482C>T (WTAPP1)
Search 100 bp 5'
Search 100 bp 3'