Canonical Allele Identifier: CA2399817861
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs1568968683
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750472T>C , CM000684.2:g.27750472T>C GRCh38
NC_000022.10:g.28146460T>C , CM000684.1:g.28146460T>C GRCh37
NC_000022.9:g.26476460T>C NCBI36
NG_023258.1:g.56027A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.931A>G
ENST00000302326.5:c.*443A>G MANE Select ENSP00000304956.4:n.*443A>G
ENST00000302326.4:c.*443A>G ENSP00000304956.4:n.*443A>G
ENST00000424656.1:c.456-244A>G
NM_002430.2:c.*443A>G NP_002421.3:n.*443A>G
NM_002430.3:c.*443A>G MANE Select NP_002421.3:n.*443A>G
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