Canonical Allele Identifier: CA476738208
Gene: MMP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102713408T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102842677T>G , CM000673.2:g.102842677T>G GRCh38
NC_000011.9:g.102713408T>G , CM000673.1:g.102713408T>G GRCh37
NC_000011.8:g.102218618T>G NCBI36
NG_012100.1:g.5935A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299855.10:c.345A>C MANE Select ENSP00000299855.5:p.Thr115=
ENST00000299855.9:c.345A>C ENSP00000299855.5:p.Thr115=
ENST00000524478.1:c.*187A>C ENSP00000435255.1:n.*187A>C
NM_002422.3:c.345A>C NP_002413.1:p.Thr115=
NM_002422.4:c.345A>C NP_002413.1:p.Thr115=
NM_002422.5:c.345A>C MANE Select NP_002413.1:p.Thr115=