Canonical Allele Identifier: CA12731523
Gene: MMP16 HGNC NCBI

Linked Data

dbSNP Id: rs1467251
gnomAD v2: 8-89272062-G-A
gnomAD v3: 8-88259833-G-A
gnomAD v4: 8-88259833-G-A
MyVariant Identifiers: chr8:g.89272062G>A (hg19) chr8:g.88259833G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88259833G>A , CM000670.2:g.88259833G>A GRCh38
NC_000008.10:g.89272062G>A , CM000670.1:g.89272062G>A GRCh37
NC_000008.9:g.89341178G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000286614.11:c.133-62527C>T MANE Select ENSP00000286614.6:n.133-62527C>T
ENST00000286614.10:c.133-62527C>T ENSP00000286614.6:n.133-62527C>T
ENST00000520568.1:n.183-62527C>T
ENST00000522726.1:c.184-62527C>T ENSP00000429147.1:n.184-62527C>T
ENST00000544227.5:n.133-62527C>T
NM_005941.4:c.133-62527C>T NP_005932.2:n.133-62527C>T
XM_011517039.1:c.133-62527C>T XP_011515341.1:n.133-62527C>T
XM_011517040.1:c.133-62527C>T XP_011515342.1:n.133-62527C>T
XM_011517042.1:c.133-62527C>T XP_011515344.1:n.133-62527C>T
XR_928334.1:n.415-62527C>T
NM_005941.5:c.133-62527C>T MANE Select NP_005932.2:n.133-62527C>T
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