Canonical Allele Identifier: CA2655934270
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750387-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750387G>T , CM000684.2:g.27750387G>T GRCh38
NC_000022.10:g.28146375G>T , CM000684.1:g.28146375G>T GRCh37
NC_000022.9:g.26476375G>T NCBI36
NG_023258.1:g.56112C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.1016C>A
ENST00000302326.5:c.*528C>A MANE Select ENSP00000304956.4:n.*528C>A
ENST00000302326.4:c.*528C>A ENSP00000304956.4:n.*528C>A
ENST00000424656.1:c.456-159C>A
NM_002430.2:c.*528C>A NP_002421.3:n.*528C>A
NM_002430.3:c.*528C>A MANE Select NP_002421.3:n.*528C>A
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