Canonical Allele Identifier: CA2655934304
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750446-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750446C>T , CM000684.2:g.27750446C>T GRCh38
NC_000022.10:g.28146434C>T , CM000684.1:g.28146434C>T GRCh37
NC_000022.9:g.26476434C>T NCBI36
NG_023258.1:g.56053G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.957G>A
ENST00000302326.5:c.*469G>A MANE Select ENSP00000304956.4:n.*469G>A
ENST00000302326.4:c.*469G>A ENSP00000304956.4:n.*469G>A
ENST00000424656.1:c.456-218G>A
NM_002430.2:c.*469G>A NP_002421.3:n.*469G>A
NM_002430.3:c.*469G>A MANE Select NP_002421.3:n.*469G>A
Search 100 bp 5'
Search 100 bp 3'