Canonical Allele Identifier: CA2655934742
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750787-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750787A>T , CM000684.2:g.27750787A>T GRCh38
NC_000022.10:g.28146775A>T , CM000684.1:g.28146775A>T GRCh37
NC_000022.9:g.26476775A>T NCBI36
NG_023258.1:g.55712T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.616T>A
ENST00000302326.5:c.*128T>A MANE Select ENSP00000304956.4:n.*128T>A
ENST00000302326.4:c.*128T>A ENSP00000304956.4:n.*128T>A
ENST00000424656.1:c.444T>A
ENST00000497225.1:n.447T>A
NM_002430.2:c.*128T>A NP_002421.3:n.*128T>A
NM_002430.3:c.*128T>A MANE Select NP_002421.3:n.*128T>A
Search 100 bp 5'
Search 100 bp 3'