Canonical Allele Identifier: CA322870589
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs891544519
MyVariant Identifiers: chr22:g.28146575T>A (hg19) chr22:g.27750587T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750587T>A , CM000684.2:g.27750587T>A GRCh38
NC_000022.10:g.28146575T>A , CM000684.1:g.28146575T>A GRCh37
NC_000022.9:g.26476575T>A NCBI36
NG_023258.1:g.55912A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.816A>T
ENST00000302326.5:c.*328A>T MANE Select ENSP00000304956.4:n.*328A>T
ENST00000302326.4:c.*328A>T ENSP00000304956.4:n.*328A>T
ENST00000424656.1:c.455+189A>T
NM_002430.2:c.*328A>T NP_002421.3:n.*328A>T
NM_002430.3:c.*328A>T MANE Select NP_002421.3:n.*328A>T
Search 100 bp 5'
Search 100 bp 3'