Canonical Allele Identifier: CA5835125
Gene: MMP26 HGNC NCBI

Linked Data

dbSNP Id: rs377281056
ExAC: 11:4790178 C / T
gnomAD v2: 11-4790178-C-T
gnomAD v3: 11-4768948-C-T
gnomAD v4: 11-4768948-C-T
MyVariant Identifiers: chr11:g.4790178C>T (hg19) chr11:g.4768948C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.4768948C>T , CM000673.2:g.4768948C>T GRCh38
NC_000011.9:g.4790178C>T , CM000673.1:g.4790178C>T GRCh37
NC_000011.8:g.4746754C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000300762.2:c.-153+1607C>T ENSP00000300762.2:n.-153+1607C>T
ENST00000380390.6:c.-145+1607C>T MANE Select ENSP00000369753.1:n.-145+1607C>T
ENST00000380390.5:c.-145+1607C>T ENSP00000369753.1:n.-145+1607C>T
ENST00000477339.5:n.191+1607C>T
NM_001384608.1:c.-153+1607C>T NP_001371537.1:n.-153+1607C>T
NM_021801.5:c.-145+1607C>T MANE Select NP_068573.2:n.-145+1607C>T
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