Canonical Allele Identifier: CA3847077
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 2004745
ClinVar RCV Id: RCV002816319
dbSNP Id: rs754026450
ExAC: 6:49425509 G / A
gnomAD v2: 6-49425509-G-A
MyVariant Identifiers: chr6:g.49425509G>A (hg19) chr6:g.49457796G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49457796G>A , CM000668.2:g.49457796G>A GRCh38
NC_000006.11:g.49425509G>A , CM000668.1:g.49425509G>A GRCh37
NC_000006.10:g.49533468G>A NCBI36
NG_007100.1:g.10344C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.648C>T MANE Select ENSP00000274813.3:p.Thr216=
ENST00000274813.3:c.648C>T ENSP00000274813.3:p.Thr216=
NM_000255.3:c.648C>T NP_000246.2:p.Thr216=
XM_005249143.2:c.648C>T XP_005249200.1:p.Thr216=
XM_005249143.3:c.648C>T XP_005249200.1:p.Thr216=
NM_000255.4:c.648C>T MANE Select NP_000246.2:p.Thr216=
Search 100 bp 5'
Search 100 bp 3'