Canonical Allele Identifier: CA638787367
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs1356807266

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750862A>T , CM000684.2:g.27750862A>T GRCh38
NC_000022.10:g.28146850A>T , CM000684.1:g.28146850A>T GRCh37
NC_000022.9:g.26476850A>T NCBI36
NG_023258.1:g.55637T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.541T>A
ENST00000302326.5:c.*53T>A MANE Select ENSP00000304956.4:n.*53T>A
ENST00000302326.4:c.*53T>A ENSP00000304956.4:n.*53T>A
ENST00000424656.1:c.369T>A
ENST00000497225.1:n.372T>A
NM_002430.2:c.*53T>A NP_002421.3:n.*53T>A
NM_002430.3:c.*53T>A MANE Select NP_002421.3:n.*53T>A