Canonical Allele Identifier: CA3847137
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 1111970
ClinVar RCV Id: RCV001438767
dbSNP Id: rs371185170
ExAC: 6:49426853 C / T
gnomAD v2: 6-49426853-C-T
gnomAD v4: 6-49459140-C-T
MyVariant Identifiers: chr6:g.49426853C>T (hg19) chr6:g.49459140C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459140C>T , CM000668.2:g.49459140C>T GRCh38
NC_000006.11:g.49426853C>T , CM000668.1:g.49426853C>T GRCh37
NC_000006.10:g.49534812C>T NCBI36
NG_007100.1:g.9000G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.327G>A MANE Select ENSP00000274813.3:p.Gln109=
ENST00000274813.3:c.327G>A ENSP00000274813.3:p.Gln109=
NM_000255.3:c.327G>A NP_000246.2:p.Gln109=
XM_005249143.2:c.327G>A XP_005249200.1:p.Gln109=
XM_005249143.3:c.327G>A XP_005249200.1:p.Gln109=
NM_000255.4:c.327G>A MANE Select NP_000246.2:p.Gln109=
Search 100 bp 5'
Search 100 bp 3'