Canonical Allele Identifier: CA2655934835
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750878-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750878G>T , CM000684.2:g.27750878G>T GRCh38
NC_000022.10:g.28146866G>T , CM000684.1:g.28146866G>T GRCh37
NC_000022.9:g.26476866G>T NCBI36
NG_023258.1:g.55621C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.525C>A
ENST00000302326.5:c.*37C>A MANE Select ENSP00000304956.4:n.*37C>A
ENST00000302326.4:c.*37C>A ENSP00000304956.4:n.*37C>A
ENST00000424656.1:c.353C>A
ENST00000497225.1:n.356C>A
NM_002430.2:c.*37C>A NP_002421.3:n.*37C>A
NM_002430.3:c.*37C>A MANE Select NP_002421.3:n.*37C>A
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