Canonical Allele Identifier: CA450608786
Gene: MMUT HGNC NCBI

Linked Data

dbSNP Id: rs1234792269
gnomAD v2: 6-49425497-A-G
gnomAD v4: 6-49457784-A-G
MyVariant Identifiers: chr6:g.49425497A>G (hg19) chr6:g.49457784A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49457784A>G , CM000668.2:g.49457784A>G GRCh38
NC_000006.11:g.49425497A>G , CM000668.1:g.49425497A>G GRCh37
NC_000006.10:g.49533456A>G NCBI36
NG_007100.1:g.10356T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.660T>C MANE Select ENSP00000274813.3:p.Asp220=
ENST00000274813.3:c.660T>C ENSP00000274813.3:p.Asp220=
NM_000255.3:c.660T>C NP_000246.2:p.Asp220=
XM_005249143.2:c.660T>C XP_005249200.1:p.Asp220=
XM_005249143.3:c.660T>C XP_005249200.1:p.Asp220=
NM_000255.4:c.660T>C MANE Select NP_000246.2:p.Asp220=
Search 100 bp 5'
Search 100 bp 3'