Canonical Allele Identifier: CA2399818038
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs1932756962
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750835G>C , CM000684.2:g.27750835G>C GRCh38
NC_000022.10:g.28146823G>C , CM000684.1:g.28146823G>C GRCh37
NC_000022.9:g.26476823G>C NCBI36
NG_023258.1:g.55664C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.568C>G
ENST00000302326.5:c.*80C>G MANE Select ENSP00000304956.4:n.*80C>G
ENST00000302326.4:c.*80C>G ENSP00000304956.4:n.*80C>G
ENST00000424656.1:c.396C>G
ENST00000497225.1:n.399C>G
NM_002430.2:c.*80C>G NP_002421.3:n.*80C>G
NM_002430.3:c.*80C>G MANE Select NP_002421.3:n.*80C>G
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