Canonical Allele Identifier: CA450609676
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 2885598
ClinVar RCV Id: RCV003717334
dbSNP Id: rs1397464862
gnomAD v4: 6-49459254-G-A
MyVariant Identifiers: chr6:g.49426967G>A (hg19) chr6:g.49459254G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459254G>A , CM000668.2:g.49459254G>A GRCh38
NC_000006.11:g.49426967G>A , CM000668.1:g.49426967G>A GRCh37
NC_000006.10:g.49534926G>A NCBI36
NG_007100.1:g.8886C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.213C>T MANE Select ENSP00000274813.3:p.Pro71=
ENST00000274813.3:c.213C>T ENSP00000274813.3:p.Pro71=
NM_000255.3:c.213C>T NP_000246.2:p.Pro71=
XM_005249143.2:c.213C>T XP_005249200.1:p.Pro71=
XM_005249143.3:c.213C>T XP_005249200.1:p.Pro71=
NM_000255.4:c.213C>T MANE Select NP_000246.2:p.Pro71=
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Search 100 bp 3'