Canonical Allele Identifier: CA450608976
Gene: MMUT HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.49427117T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459404T>C , CM000668.2:g.49459404T>C GRCh38
NC_000006.11:g.49427117T>C , CM000668.1:g.49427117T>C GRCh37
NC_000006.10:g.49535076T>C NCBI36
NG_007100.1:g.8736A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.63A>G MANE Select ENSP00000274813.3:p.Glu21=
ENST00000274813.3:c.63A>G ENSP00000274813.3:p.Glu21=
NM_000255.3:c.63A>G NP_000246.2:p.Glu21=
XM_005249143.2:c.63A>G XP_005249200.1:p.Glu21=
XM_005249143.3:c.63A>G XP_005249200.1:p.Glu21=
NM_000255.4:c.63A>G MANE Select NP_000246.2:p.Glu21=