Canonical Allele Identifier: CA364405997
Gene: MMUT HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.49427155A>C (hg19) chr6:g.49459442A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459442A>C , CM000668.2:g.49459442A>C GRCh38
NC_000006.11:g.49427155A>C , CM000668.1:g.49427155A>C GRCh37
NC_000006.10:g.49535114A>C NCBI36
NG_007100.1:g.8698T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.25T>G MANE Select ENSP00000274813.3:p.Phe9Val
ENST00000274813.3:c.25T>G ENSP00000274813.3:p.Phe9Val
NM_000255.3:c.25T>G NP_000246.2:p.Phe9Val
XM_005249143.2:c.25T>G XP_005249200.1:p.Phe9Val
XM_005249143.3:c.25T>G XP_005249200.1:p.Phe9Val
NM_000255.4:c.25T>G MANE Select NP_000246.2:p.Phe9Val
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