Canonical Allele Identifier: CA12731493

Gene: MMP16

Linked Data

• dbSNP Id: rs1824717
• gnomAD v2: 8-89075979-T-C
• gnomAD v3: 8-88063751-T-C
• gnomAD v4: 8-88063751-T-C
• MyVariant Identifiers: chr8:g.89075979T>C (hg19) ; chr8:g.88063751T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88063751T>C , CM000670.2:g.88063751T>C	GRCh38
NC_000008.10:g.89075979T>C , CM000670.1:g.89075979T>C	GRCh37
NC_000008.9:g.89145095T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286614.11:c.1223-7473A>G MANE Select	ENSP00000286614.6:n.1223-7473A>G
ENST00000286614.10:c.1223-7473A>G	ENSP00000286614.6:n.1223-7473A>G
NM_005941.4:c.1223-7473A>G	NP_005932.2:n.1223-7473A>G
XM_011517039.1:c.1223-7473A>G	XP_011515341.1:n.1223-7473A>G
XM_011517040.1:c.1223-7473A>G	XP_011515342.1:n.1223-7473A>G
XM_011517041.1:c.1094-7473A>G	XP_011515343.1:n.1094-7473A>G
XR_928334.1:n.1505-7473A>G
XM_024447154.1:c.434-7473A>G	XP_024302922.1:n.434-7473A>G
NM_005941.5:c.1223-7473A>G MANE Select	NP_005932.2:n.1223-7473A>G