Canonical Allele Identifier: CA513939238
Gene: MN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.28146927C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750939C>T , CM000684.2:g.27750939C>T GRCh38
NC_000022.10:g.28146927C>T , CM000684.1:g.28146927C>T GRCh37
NC_000022.9:g.26476927C>T NCBI36
NG_023258.1:g.55560G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.464G>A
ENST00000302326.5:c.3939G>A MANE Select ENSP00000304956.4:p.Gly1313=
ENST00000302326.4:c.3939G>A ENSP00000304956.4:p.Gly1313=
ENST00000424656.1:c.292G>A
ENST00000497225.1:n.295G>A
NM_002430.2:c.3939G>A NP_002421.3:p.Gly1313=
NM_002430.3:c.3939G>A MANE Select NP_002421.3:p.Gly1313=