Canonical Allele Identifier: CA2399817985
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs765470413
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750727C>G , CM000684.2:g.27750727C>G GRCh38
NC_000022.10:g.28146715C>G , CM000684.1:g.28146715C>G GRCh37
NC_000022.9:g.26476715C>G NCBI36
NG_023258.1:g.55772G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.676G>C
ENST00000302326.5:c.*188G>C MANE Select ENSP00000304956.4:n.*188G>C
ENST00000302326.4:c.*188G>C ENSP00000304956.4:n.*188G>C
ENST00000424656.1:c.455+49G>C
ENST00000497225.1:n.507G>C
NM_002430.2:c.*188G>C NP_002421.3:n.*188G>C
NM_002430.3:c.*188G>C MANE Select NP_002421.3:n.*188G>C
Search 100 bp 5'
Search 100 bp 3'