Canonical Allele Identifier: CA138795476
Gene: MMUT HGNC NCBI

Linked Data

dbSNP Id: rs1051319765
gnomAD v4: 6-49444493-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49444493G>A , CM000668.2:g.49444493G>A GRCh38
NC_000006.11:g.49412206G>A , CM000668.1:g.49412206G>A GRCh37
NC_000006.10:g.49520165G>A NCBI36
NG_007100.1:g.23647C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1676+146C>T MANE Select ENSP00000274813.3:n.1676+146C>T
ENST00000274813.3:c.1676+146C>T ENSP00000274813.3:n.1676+146C>T
NM_000255.3:c.1676+146C>T NP_000246.2:n.1676+146C>T
XM_005249143.2:c.1676+146C>T XP_005249200.1:n.1676+146C>T
XM_005249143.3:c.1676+146C>T XP_005249200.1:n.1676+146C>T
NM_000255.4:c.1676+146C>T MANE Select NP_000246.2:n.1676+146C>T