Canonical Allele Identifier: CA2655934385
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750615-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750615T>A , CM000684.2:g.27750615T>A GRCh38
NC_000022.10:g.28146603T>A , CM000684.1:g.28146603T>A GRCh37
NC_000022.9:g.26476603T>A NCBI36
NG_023258.1:g.55884A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.788A>T
ENST00000302326.5:c.*300A>T MANE Select ENSP00000304956.4:n.*300A>T
ENST00000302326.4:c.*300A>T ENSP00000304956.4:n.*300A>T
ENST00000424656.1:c.455+161A>T
NM_002430.2:c.*300A>T NP_002421.3:n.*300A>T
NM_002430.3:c.*300A>T MANE Select NP_002421.3:n.*300A>T
Search 100 bp 5'
Search 100 bp 3'