Canonical Allele Identifier: CA3847138
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 718015
ClinVar RCV Id: RCV000890896 RCV001271805
dbSNP Id: rs570459486
ExAC: 6:49426859 G / A
gnomAD v2: 6-49426859-G-A
gnomAD v3: 6-49459146-G-A
gnomAD v4: 6-49459146-G-A
COSMIC: COSM6356566
MyVariant Identifiers: chr6:g.49426859G>A (hg19) chr6:g.49459146G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459146G>A , CM000668.2:g.49459146G>A GRCh38
NC_000006.11:g.49426859G>A , CM000668.1:g.49426859G>A GRCh37
NC_000006.10:g.49534818G>A NCBI36
NG_007100.1:g.8994C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.321C>T MANE Select ENSP00000274813.3:p.Ile107=
ENST00000274813.3:c.321C>T ENSP00000274813.3:p.Ile107=
NM_000255.3:c.321C>T NP_000246.2:p.Ile107=
XM_005249143.2:c.321C>T XP_005249200.1:p.Ile107=
XM_005249143.3:c.321C>T XP_005249200.1:p.Ile107=
NM_000255.4:c.321C>T MANE Select NP_000246.2:p.Ile107=
Search 100 bp 5'
Search 100 bp 3'