Canonical Allele Identifier: CA2655934814
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750845-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750845A>G , CM000684.2:g.27750845A>G GRCh38
NC_000022.10:g.28146833A>G , CM000684.1:g.28146833A>G GRCh37
NC_000022.9:g.26476833A>G NCBI36
NG_023258.1:g.55654T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.558T>C
ENST00000302326.5:c.*70T>C MANE Select ENSP00000304956.4:n.*70T>C
ENST00000302326.4:c.*70T>C ENSP00000304956.4:n.*70T>C
ENST00000424656.1:c.386T>C
ENST00000497225.1:n.389T>C
NM_002430.2:c.*70T>C NP_002421.3:n.*70T>C
NM_002430.3:c.*70T>C MANE Select NP_002421.3:n.*70T>C
Search 100 bp 5'
Search 100 bp 3'