Canonical Allele Identifier: CA364397258

Gene: MMUT

Linked Data

• gnomAD v4: 6-49447756-A-G
• MyVariant Identifiers: chr6:g.49415469A>G (hg19) ; chr6:g.49447756A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49447756A>G , CM000668.2:g.49447756A>G	GRCh38
NC_000006.11:g.49415469A>G , CM000668.1:g.49415469A>G	GRCh37
NC_000006.10:g.49523428A>G	NCBI36
NG_007100.1:g.20384T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1474T>C MANE Select	ENSP00000274813.3:p.Tyr492His
ENST00000274813.3:c.1474T>C	ENSP00000274813.3:p.Tyr492His
NM_000255.3:c.1474T>C	NP_000246.2:p.Tyr492His
XM_005249143.2:c.1474T>C	XP_005249200.1:p.Tyr492His
XM_005249143.3:c.1474T>C	XP_005249200.1:p.Tyr492His
NM_000255.4:c.1474T>C MANE Select	NP_000246.2:p.Tyr492His