Canonical Allele Identifier: CA411033644
Gene: MN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.28147046G>T (hg19) chr22:g.27751058G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27751058G>T , CM000684.2:g.27751058G>T GRCh38
NC_000022.10:g.28147046G>T , CM000684.1:g.28147046G>T GRCh37
NC_000022.9:g.26477046G>T NCBI36
NG_023258.1:g.55441C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.345C>A
ENST00000302326.5:c.3820C>A MANE Select ENSP00000304956.4:p.Pro1274Thr
ENST00000302326.4:c.3820C>A ENSP00000304956.4:p.Pro1274Thr
ENST00000424656.1:c.173C>A
ENST00000497225.1:n.176C>A
NM_002430.2:c.3820C>A NP_002421.3:p.Pro1274Thr
NM_002430.3:c.3820C>A MANE Select NP_002421.3:p.Pro1274Thr
Search 100 bp 5'
Search 100 bp 3'