Canonical Allele Identifier: CA2399818000
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs1932756288
gnomAD v4: 22-27750760-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750760C>T , CM000684.2:g.27750760C>T GRCh38
NC_000022.10:g.28146748C>T , CM000684.1:g.28146748C>T GRCh37
NC_000022.9:g.26476748C>T NCBI36
NG_023258.1:g.55739G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.643G>A
ENST00000302326.5:c.*155G>A MANE Select ENSP00000304956.4:n.*155G>A
ENST00000302326.4:c.*155G>A ENSP00000304956.4:n.*155G>A
ENST00000424656.1:c.455+16G>A
ENST00000497225.1:n.474G>A
NM_002430.2:c.*155G>A NP_002421.3:n.*155G>A
NM_002430.3:c.*155G>A MANE Select NP_002421.3:n.*155G>A
Search 100 bp 5'
Search 100 bp 3'