Canonical Allele Identifier: CA450609593
Gene: MMUT HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.49426910T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459197T>A , CM000668.2:g.49459197T>A GRCh38
NC_000006.11:g.49426910T>A , CM000668.1:g.49426910T>A GRCh37
NC_000006.10:g.49534869T>A NCBI36
NG_007100.1:g.8943A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.270A>T MANE Select ENSP00000274813.3:p.Pro90=
ENST00000274813.3:c.270A>T ENSP00000274813.3:p.Pro90=
NM_000255.3:c.270A>T NP_000246.2:p.Pro90=
XM_005249143.2:c.270A>T XP_005249200.1:p.Pro90=
XM_005249143.3:c.270A>T XP_005249200.1:p.Pro90=
NM_000255.4:c.270A>T MANE Select NP_000246.2:p.Pro90=