Canonical Allele Identifier: CA1024815432
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v3: 22-27750446-C-A
gnomAD v4: 22-27750446-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750446C>A , CM000684.2:g.27750446C>A GRCh38
NC_000022.10:g.28146434C>A , CM000684.1:g.28146434C>A GRCh37
NC_000022.9:g.26476434C>A NCBI36
NG_023258.1:g.56053G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.957G>T
ENST00000302326.5:c.*469G>T MANE Select ENSP00000304956.4:n.*469G>T
ENST00000302326.4:c.*469G>T ENSP00000304956.4:n.*469G>T
ENST00000424656.1:c.456-218G>T
NM_002430.2:c.*469G>T NP_002421.3:n.*469G>T
NM_002430.3:c.*469G>T MANE Select NP_002421.3:n.*469G>T
Search 100 bp 5'
Search 100 bp 3'