Canonical Allele Identifier: CA2655934837
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750880-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750880A>G , CM000684.2:g.27750880A>G GRCh38
NC_000022.10:g.28146868A>G , CM000684.1:g.28146868A>G GRCh37
NC_000022.9:g.26476868A>G NCBI36
NG_023258.1:g.55619T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.523T>C
ENST00000302326.5:c.*35T>C MANE Select ENSP00000304956.4:n.*35T>C
ENST00000302326.4:c.*35T>C ENSP00000304956.4:n.*35T>C
ENST00000424656.1:c.351T>C
ENST00000497225.1:n.354T>C
NM_002430.2:c.*35T>C NP_002421.3:n.*35T>C
NM_002430.3:c.*35T>C MANE Select NP_002421.3:n.*35T>C
Search 100 bp 5'
Search 100 bp 3'