Canonical Allele Identifier: CA364405444
Gene: MMUT HGNC NCBI

Linked Data

dbSNP Id: rs1767776360
gnomAD v3: 6-49459279-G-T
gnomAD v4: 6-49459279-G-T
MyVariant Identifiers: chr6:g.49426992G>T (hg19) chr6:g.49459279G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459279G>T , CM000668.2:g.49459279G>T GRCh38
NC_000006.11:g.49426992G>T , CM000668.1:g.49426992G>T GRCh37
NC_000006.10:g.49534951G>T NCBI36
NG_007100.1:g.8861C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.188C>A MANE Select ENSP00000274813.3:p.Thr63Asn
ENST00000274813.3:c.188C>A ENSP00000274813.3:p.Thr63Asn
NM_000255.3:c.188C>A NP_000246.2:p.Thr63Asn
XM_005249143.2:c.188C>A XP_005249200.1:p.Thr63Asn
XM_005249143.3:c.188C>A XP_005249200.1:p.Thr63Asn
NM_000255.4:c.188C>A MANE Select NP_000246.2:p.Thr63Asn
Search 100 bp 5'
Search 100 bp 3'