Canonical Allele Identifier: CA2399817908
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs1932754596
gnomAD v4: 22-27750564-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750564G>A , CM000684.2:g.27750564G>A GRCh38
NC_000022.10:g.28146552G>A , CM000684.1:g.28146552G>A GRCh37
NC_000022.9:g.26476552G>A NCBI36
NG_023258.1:g.55935C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.839C>T
ENST00000302326.5:c.*351C>T MANE Select ENSP00000304956.4:n.*351C>T
ENST00000302326.4:c.*351C>T ENSP00000304956.4:n.*351C>T
ENST00000424656.1:c.455+212C>T
NM_002430.2:c.*351C>T NP_002421.3:n.*351C>T
NM_002430.3:c.*351C>T MANE Select NP_002421.3:n.*351C>T
Search 100 bp 5'
Search 100 bp 3'