Canonical Allele Identifier: CA2655934734
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750783-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750783A>C , CM000684.2:g.27750783A>C GRCh38
NC_000022.10:g.28146771A>C , CM000684.1:g.28146771A>C GRCh37
NC_000022.9:g.26476771A>C NCBI36
NG_023258.1:g.55716T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.620T>G
ENST00000302326.5:c.*132T>G MANE Select ENSP00000304956.4:n.*132T>G
ENST00000302326.4:c.*132T>G ENSP00000304956.4:n.*132T>G
ENST00000424656.1:c.448T>G
ENST00000497225.1:n.451T>G
NM_002430.2:c.*132T>G NP_002421.3:n.*132T>G
NM_002430.3:c.*132T>G MANE Select NP_002421.3:n.*132T>G
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