Canonical Allele Identifier: CA364398921
Gene: MMUT HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.49419319T>A (hg19) chr6:g.49451606T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49451606T>A , CM000668.2:g.49451606T>A GRCh38
NC_000006.11:g.49419319T>A , CM000668.1:g.49419319T>A GRCh37
NC_000006.10:g.49527278T>A NCBI36
NG_007100.1:g.16534A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.1192A>T MANE Select ENSP00000274813.3:p.Thr398Ser
ENST00000274813.3:c.1192A>T ENSP00000274813.3:p.Thr398Ser
NM_000255.3:c.1192A>T NP_000246.2:p.Thr398Ser
XM_005249143.2:c.1192A>T XP_005249200.1:p.Thr398Ser
XM_005249143.3:c.1192A>T XP_005249200.1:p.Thr398Ser
NM_000255.4:c.1192A>T MANE Select NP_000246.2:p.Thr398Ser
Search 100 bp 5'
Search 100 bp 3'