Canonical Allele Identifier: CA2399818029
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs1601319364
gnomAD v4: 22-27750810-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750810T>C , CM000684.2:g.27750810T>C GRCh38
NC_000022.10:g.28146798T>C , CM000684.1:g.28146798T>C GRCh37
NC_000022.9:g.26476798T>C NCBI36
NG_023258.1:g.55689A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.593A>G
ENST00000302326.5:c.*105A>G MANE Select ENSP00000304956.4:n.*105A>G
ENST00000302326.4:c.*105A>G ENSP00000304956.4:n.*105A>G
ENST00000424656.1:c.421A>G
ENST00000497225.1:n.424A>G
NM_002430.2:c.*105A>G NP_002421.3:n.*105A>G
NM_002430.3:c.*105A>G MANE Select NP_002421.3:n.*105A>G
Search 100 bp 5'
Search 100 bp 3'