Canonical Allele Identifier: CA450609601

Gene: MMUT

Linked Data

• MyVariant Identifiers: chr6:g.49426916C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459203C>G , CM000668.2:g.49459203C>G	GRCh38
NC_000006.11:g.49426916C>G , CM000668.1:g.49426916C>G	GRCh37
NC_000006.10:g.49534875C>G	NCBI36
NG_007100.1:g.8937G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.264G>C MANE Select	ENSP00000274813.3:p.Val88=
ENST00000274813.3:c.264G>C	ENSP00000274813.3:p.Val88=
NM_000255.3:c.264G>C	NP_000246.2:p.Val88=
XM_005249143.2:c.264G>C	XP_005249200.1:p.Val88=
XM_005249143.3:c.264G>C	XP_005249200.1:p.Val88=
NM_000255.4:c.264G>C MANE Select	NP_000246.2:p.Val88=