Canonical Allele Identifier: CA450399713
Gene: MMUT HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.49426847A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459134A>T , CM000668.2:g.49459134A>T GRCh38
NC_000006.11:g.49426847A>T , CM000668.1:g.49426847A>T GRCh37
NC_000006.10:g.49534806A>T NCBI36
NG_007100.1:g.9006T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.333T>A MANE Select ENSP00000274813.3:p.Ala111=
ENST00000274813.3:c.333T>A ENSP00000274813.3:p.Ala111=
NM_000255.3:c.333T>A NP_000246.2:p.Ala111=
XM_005249143.2:c.333T>A XP_005249200.1:p.Ala111=
XM_005249143.3:c.333T>A XP_005249200.1:p.Ala111=
NM_000255.4:c.333T>A MANE Select NP_000246.2:p.Ala111=