Canonical Allele Identifier: CA364405089
Gene: MMUT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459187C>G , CM000668.2:g.49459187C>G GRCh38
NC_000006.11:g.49426900C>G , CM000668.1:g.49426900C>G GRCh37
NC_000006.10:g.49534859C>G NCBI36
NG_007100.1:g.8953G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.280G>C MANE Select ENSP00000274813.3:p.Gly94Arg
ENST00000274813.3:c.280G>C ENSP00000274813.3:p.Gly94Arg
NM_000255.3:c.280G>C NP_000246.2:p.Gly94Arg
XM_005249143.2:c.280G>C XP_005249200.1:p.Gly94Arg
XM_005249143.3:c.280G>C XP_005249200.1:p.Gly94Arg
NM_000255.4:c.280G>C MANE Select NP_000246.2:p.Gly94Arg