Canonical Allele Identifier: CA1627396964
Gene: MMUT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459280T= , CM000668.2:g.49459280T= GRCh38
NC_000006.11:g.49426993T= , CM000668.1:g.49426993T= GRCh37
NC_000006.10:g.49534952T= NCBI36
NG_007100.1:g.8860A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.187A= MANE Select ENSP00000274813.3:p.Thr63=
ENST00000274813.3:c.187A= ENSP00000274813.3:p.Thr63=
NM_000255.3:c.187A= NP_000246.2:p.Thr63=
XM_005249143.2:c.187A= XP_005249200.1:p.Thr63=
XM_005249143.3:c.187A= XP_005249200.1:p.Thr63=
NM_000255.4:c.187A= MANE Select NP_000246.2:p.Thr63=
Search 100 bp 5'
Search 100 bp 3'