Canonical Allele Identifier: CA15677224
Gene: MMP8 HGNC NCBI

Linked Data

dbSNP Id: rs11225395

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102725749A>G , CM000673.2:g.102725749A>G GRCh38
NC_000011.9:g.102596480A>G , CM000673.1:g.102596480A>G GRCh37
NC_000011.8:g.102101690A>G NCBI36
NG_012101.1:g.4206T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000528662.6:c.-148-746T>C ENSP00000431431.2:n.-148-746T>C