Canonical Allele Identifier: CA364404987
Gene: MMUT HGNC NCBI

Linked Data

gnomAD v4: 6-49459139-A-G
MyVariant Identifiers: chr6:g.49426852A>G (hg19) chr6:g.49459139A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459139A>G , CM000668.2:g.49459139A>G GRCh38
NC_000006.11:g.49426852A>G , CM000668.1:g.49426852A>G GRCh37
NC_000006.10:g.49534811A>G NCBI36
NG_007100.1:g.9001T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.328T>C MANE Select ENSP00000274813.3:p.Tyr110His
ENST00000274813.3:c.328T>C ENSP00000274813.3:p.Tyr110His
NM_000255.3:c.328T>C NP_000246.2:p.Tyr110His
XM_005249143.2:c.328T>C XP_005249200.1:p.Tyr110His
XM_005249143.3:c.328T>C XP_005249200.1:p.Tyr110His
NM_000255.4:c.328T>C MANE Select NP_000246.2:p.Tyr110His
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