Canonical Allele Identifier: CA364397286
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 1487103
ClinVar RCV Id: RCV002033461
dbSNP Id: rs1767446389
COSMIC: COSM6367019
MyVariant Identifiers: chr6:g.49415484C>A (hg19) chr6:g.49447771C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447771C>A , CM000668.2:g.49447771C>A GRCh38
NC_000006.11:g.49415484C>A , CM000668.1:g.49415484C>A GRCh37
NC_000006.10:g.49523443C>A NCBI36
NG_007100.1:g.20369G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1459G>T MANE Select ENSP00000274813.3:p.Val487Phe
ENST00000274813.3:c.1459G>T ENSP00000274813.3:p.Val487Phe
NM_000255.3:c.1459G>T NP_000246.2:p.Val487Phe
XM_005249143.2:c.1459G>T XP_005249200.1:p.Val487Phe
XM_005249143.3:c.1459G>T XP_005249200.1:p.Val487Phe
NM_000255.4:c.1459G>T MANE Select NP_000246.2:p.Val487Phe
Search 100 bp 5'
Search 100 bp 3'