Canonical Allele Identifier: CA2655934312
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750469-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750469G>T , CM000684.2:g.27750469G>T GRCh38
NC_000022.10:g.28146457G>T , CM000684.1:g.28146457G>T GRCh37
NC_000022.9:g.26476457G>T NCBI36
NG_023258.1:g.56030C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.934C>A
ENST00000302326.5:c.*446C>A MANE Select ENSP00000304956.4:n.*446C>A
ENST00000302326.4:c.*446C>A ENSP00000304956.4:n.*446C>A
ENST00000424656.1:c.456-241C>A
NM_002430.2:c.*446C>A NP_002421.3:n.*446C>A
NM_002430.3:c.*446C>A MANE Select NP_002421.3:n.*446C>A
Search 100 bp 5'
Search 100 bp 3'