Canonical Allele Identifier: CA411032960
Gene: MN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.28146956G>T (hg19) chr22:g.27750968G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750968G>T , CM000684.2:g.27750968G>T GRCh38
NC_000022.10:g.28146956G>T , CM000684.1:g.28146956G>T GRCh37
NC_000022.9:g.26476956G>T NCBI36
NG_023258.1:g.55531C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.435C>A
ENST00000302326.5:c.3910C>A MANE Select ENSP00000304956.4:p.Leu1304Met
ENST00000302326.4:c.3910C>A ENSP00000304956.4:p.Leu1304Met
ENST00000424656.1:c.263C>A
ENST00000497225.1:n.266C>A
NM_002430.2:c.3910C>A NP_002421.3:p.Leu1304Met
NM_002430.3:c.3910C>A MANE Select NP_002421.3:p.Leu1304Met
Search 100 bp 5'
Search 100 bp 3'