Canonical Allele Identifier: CA3846880
Gene: MMUT HGNC NCBI

Linked Data

dbSNP Id: rs760632896
gnomAD v2: 6-49416483-C-A
gnomAD v3: 6-49448770-C-A
gnomAD v4: 6-49448770-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49448770C>A , CM000668.2:g.49448770C>A GRCh38
NC_000006.11:g.49416483C>A , CM000668.1:g.49416483C>A GRCh37
NC_000006.10:g.49524442C>A NCBI36
NG_007100.1:g.19370G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1444+46G>T MANE Select ENSP00000274813.3:n.1444+46G>T
ENST00000274813.3:c.1444+46G>T ENSP00000274813.3:n.1444+46G>T
NM_000255.3:c.1444+46G>T NP_000246.2:n.1444+46G>T
XM_005249143.2:c.1444+46G>T XP_005249200.1:n.1444+46G>T
XM_005249143.3:c.1444+46G>T XP_005249200.1:n.1444+46G>T
NM_000255.4:c.1444+46G>T MANE Select NP_000246.2:n.1444+46G>T