Canonical Allele Identifier: CA364405039

Gene: MMUT

Linked Data

• dbSNP Id: rs1767770117
• MyVariant Identifiers: chr6:g.49426876A>C (hg19) ; chr6:g.49459163A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459163A>C , CM000668.2:g.49459163A>C	GRCh38
NC_000006.11:g.49426876A>C , CM000668.1:g.49426876A>C	GRCh37
NC_000006.10:g.49534835A>C	NCBI36
NG_007100.1:g.8977T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.304T>G MANE Select	ENSP00000274813.3:p.Phe102Val
ENST00000274813.3:c.304T>G	ENSP00000274813.3:p.Phe102Val
NM_000255.3:c.304T>G	NP_000246.2:p.Phe102Val
XM_005249143.2:c.304T>G	XP_005249200.1:p.Phe102Val
XM_005249143.3:c.304T>G	XP_005249200.1:p.Phe102Val
NM_000255.4:c.304T>G MANE Select	NP_000246.2:p.Phe102Val