Canonical Allele Identifier: CA567155983
Gene: MMUT HGNC NCBI

Linked Data

dbSNP Id: rs1336174779
gnomAD v2: 6-49425806-G-A
gnomAD v4: 6-49458093-G-A
MyVariant Identifiers: chr6:g.49425806G>A (hg19) chr6:g.49458093G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49458093G>A , CM000668.2:g.49458093G>A GRCh38
NC_000006.11:g.49425806G>A , CM000668.1:g.49425806G>A GRCh37
NC_000006.10:g.49533765G>A NCBI36
NG_007100.1:g.10047C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.386-35C>T MANE Select ENSP00000274813.3:n.386-35C>T
ENST00000274813.3:c.386-35C>T ENSP00000274813.3:n.386-35C>T
NM_000255.3:c.386-35C>T NP_000246.2:n.386-35C>T
XM_005249143.2:c.386-35C>T XP_005249200.1:n.386-35C>T
XM_005249143.3:c.386-35C>T XP_005249200.1:n.386-35C>T
NM_000255.4:c.386-35C>T MANE Select NP_000246.2:n.386-35C>T
Search 100 bp 5'
Search 100 bp 3'