Canonical Allele Identifier: CA450609517
Gene: MMUT HGNC NCBI

Linked Data

gnomAD v4: 6-49459158-C-T
MyVariant Identifiers: chr6:g.49426871C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459158C>T , CM000668.2:g.49459158C>T GRCh38
NC_000006.11:g.49426871C>T , CM000668.1:g.49426871C>T GRCh37
NC_000006.10:g.49534830C>T NCBI36
NG_007100.1:g.8982G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.309G>A MANE Select ENSP00000274813.3:p.Arg103=
ENST00000274813.3:c.309G>A ENSP00000274813.3:p.Arg103=
NM_000255.3:c.309G>A NP_000246.2:p.Arg103=
XM_005249143.2:c.309G>A XP_005249200.1:p.Arg103=
XM_005249143.3:c.309G>A XP_005249200.1:p.Arg103=
NM_000255.4:c.309G>A MANE Select NP_000246.2:p.Arg103=