Canonical Allele Identifier: CA856503489

Gene: MMP16

Linked Data

• dbSNP Id: rs1477122169
• gnomAD v3: 8-88076976-A-G
• gnomAD v4: 8-88076976-A-G
• MyVariant Identifiers: chr8:g.89089204A>G (hg19) ; chr8:g.88076976A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88076976A>G , CM000670.2:g.88076976A>G	GRCh38
NC_000008.10:g.89089204A>G , CM000670.1:g.89089204A>G	GRCh37
NC_000008.9:g.89158320A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286614.11:c.1084-2233T>C MANE Select	ENSP00000286614.6:n.1084-2233T>C
ENST00000286614.10:c.1084-2233T>C	ENSP00000286614.6:n.1084-2233T>C
ENST00000544227.5:n.1084-2233T>C
NM_005941.4:c.1084-2233T>C	NP_005932.2:n.1084-2233T>C
XM_011517039.1:c.1084-2233T>C	XP_011515341.1:n.1084-2233T>C
XM_011517040.1:c.1084-2233T>C	XP_011515342.1:n.1084-2233T>C
XM_011517041.1:c.955-2233T>C	XP_011515343.1:n.955-2233T>C
XM_011517042.1:c.1084-2233T>C	XP_011515344.1:n.1084-2233T>C
XR_928334.1:n.1366-2233T>C
XM_024447154.1:c.295-2233T>C	XP_024302922.1:n.295-2233T>C
NM_005941.5:c.1084-2233T>C MANE Select	NP_005932.2:n.1084-2233T>C