Canonical Allele Identifier: CA3847130

Gene: MMUT

Linked Data

• dbSNP Id: rs773507404
• ExAC: 6:49426780 A / C
• gnomAD v2: 6-49426780-A-C
• gnomAD v4: 6-49459067-A-C
• MyVariant Identifiers: chr6:g.49426780A>C (hg19) ; chr6:g.49459067A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459067A>C , CM000668.2:g.49459067A>C	GRCh38
NC_000006.11:g.49426780A>C , CM000668.1:g.49426780A>C	GRCh37
NC_000006.10:g.49534739A>C	NCBI36
NG_007100.1:g.9073T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000274813.4:c.385+15T>G MANE Select	ENSP00000274813.3:n.385+15T>G
ENST00000274813.3:c.385+15T>G	ENSP00000274813.3:n.385+15T>G
NM_000255.3:c.385+15T>G	NP_000246.2:n.385+15T>G
XM_005249143.2:c.385+15T>G	XP_005249200.1:n.385+15T>G
XM_005249143.3:c.385+15T>G	XP_005249200.1:n.385+15T>G
NM_000255.4:c.385+15T>G MANE Select	NP_000246.2:n.385+15T>G