Canonical Allele Identifier: CA476738298

Gene: MMP3

Linked Data

• MyVariant Identifiers: chr11:g.102713452T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102842721T>G , CM000673.2:g.102842721T>G	GRCh38
NC_000011.9:g.102713452T>G , CM000673.1:g.102713452T>G	GRCh37
NC_000011.8:g.102218662T>G	NCBI36
NG_012100.1:g.5891A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299855.10:c.301A>C MANE Select	ENSP00000299855.5:p.Arg101=
ENST00000299855.9:c.301A>C	ENSP00000299855.5:p.Arg101=
ENST00000524478.1:c.*143A>C	ENSP00000435255.1:n.*143A>C
NM_002422.3:c.301A>C	NP_002413.1:p.Arg101=
NM_002422.4:c.301A>C	NP_002413.1:p.Arg101=
NM_002422.5:c.301A>C MANE Select	NP_002413.1:p.Arg101=