Canonical Allele Identifier: CA450609544

Gene: MMUT

Linked Data

• MyVariant Identifiers: chr6:g.49426886G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459173G>T , CM000668.2:g.49459173G>T	GRCh38
NC_000006.11:g.49426886G>T , CM000668.1:g.49426886G>T	GRCh37
NC_000006.10:g.49534845G>T	NCBI36
NG_007100.1:g.8967C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.294C>A MANE Select	ENSP00000274813.3:p.Thr98=
ENST00000274813.3:c.294C>A	ENSP00000274813.3:p.Thr98=
NM_000255.3:c.294C>A	NP_000246.2:p.Thr98=
XM_005249143.2:c.294C>A	XP_005249200.1:p.Thr98=
XM_005249143.3:c.294C>A	XP_005249200.1:p.Thr98=
NM_000255.4:c.294C>A MANE Select	NP_000246.2:p.Thr98=