Canonical Allele Identifier: CA411032679
Gene: MN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.28146903T>C (hg19) chr22:g.27750915T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750915T>C , CM000684.2:g.27750915T>C GRCh38
NC_000022.10:g.28146903T>C , CM000684.1:g.28146903T>C GRCh37
NC_000022.9:g.26476903T>C NCBI36
NG_023258.1:g.55584A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.488A>G
ENST00000302326.5:c.3963A>G MANE Select ENSP00000304956.4:p.Ter1321Trp
ENST00000302326.4:c.3963A>G ENSP00000304956.4:p.Ter1321Trp
ENST00000424656.1:c.316A>G
ENST00000497225.1:n.319A>G
NM_002430.2:c.3963A>G NP_002421.3:p.Ter1321Trp
NM_002430.3:c.3963A>G MANE Select NP_002421.3:p.Ter1321Trp
Search 100 bp 5'
Search 100 bp 3'