Canonical Allele Identifier: CA138795808

Gene: MMUT

Linked Data

• dbSNP Id: rs561697133
• gnomAD v2: 6-49415701-G-A
• gnomAD v3: 6-49447988-G-A
• gnomAD v4: 6-49447988-G-A
• MyVariant Identifiers: chr6:g.49415701G>A (hg19) ; chr6:g.49447988G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49447988G>A , CM000668.2:g.49447988G>A	GRCh38
NC_000006.11:g.49415701G>A , CM000668.1:g.49415701G>A	GRCh37
NC_000006.10:g.49523660G>A	NCBI36
NG_007100.1:g.20152C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1445-203C>T MANE Select	ENSP00000274813.3:n.1445-203C>T
ENST00000274813.3:c.1445-203C>T	ENSP00000274813.3:n.1445-203C>T
NM_000255.3:c.1445-203C>T	NP_000246.2:n.1445-203C>T
XM_005249143.2:c.1445-203C>T	XP_005249200.1:n.1445-203C>T
XM_005249143.3:c.1445-203C>T	XP_005249200.1:n.1445-203C>T
NM_000255.4:c.1445-203C>T MANE Select	NP_000246.2:n.1445-203C>T