Canonical Allele Identifier: CA2655934436
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750695-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750695T>G , CM000684.2:g.27750695T>G GRCh38
NC_000022.10:g.28146683T>G , CM000684.1:g.28146683T>G GRCh37
NC_000022.9:g.26476683T>G NCBI36
NG_023258.1:g.55804A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.708A>C
ENST00000302326.5:c.*220A>C MANE Select ENSP00000304956.4:n.*220A>C
ENST00000302326.4:c.*220A>C ENSP00000304956.4:n.*220A>C
ENST00000424656.1:c.455+81A>C
ENST00000497225.1:n.539A>C
NM_002430.2:c.*220A>C NP_002421.3:n.*220A>C
NM_002430.3:c.*220A>C MANE Select NP_002421.3:n.*220A>C
Search 100 bp 5'
Search 100 bp 3'