Canonical Allele Identifier: CA450609958
Gene: MMUT HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.49427114T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459401T>G , CM000668.2:g.49459401T>G GRCh38
NC_000006.11:g.49427114T>G , CM000668.1:g.49427114T>G GRCh37
NC_000006.10:g.49535073T>G NCBI36
NG_007100.1:g.8739A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.66A>C MANE Select ENSP00000274813.3:p.Ser22=
ENST00000274813.3:c.66A>C ENSP00000274813.3:p.Ser22=
NM_000255.3:c.66A>C NP_000246.2:p.Ser22=
XM_005249143.2:c.66A>C XP_005249200.1:p.Ser22=
XM_005249143.3:c.66A>C XP_005249200.1:p.Ser22=
NM_000255.4:c.66A>C MANE Select NP_000246.2:p.Ser22=