Canonical Allele Identifier: CA411032967
Gene: MN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.28146958G>T (hg19) chr22:g.27750970G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750970G>T , CM000684.2:g.27750970G>T GRCh38
NC_000022.10:g.28146958G>T , CM000684.1:g.28146958G>T GRCh37
NC_000022.9:g.26476958G>T NCBI36
NG_023258.1:g.55529C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.433C>A
ENST00000302326.5:c.3908C>A MANE Select ENSP00000304956.4:p.Ser1303Tyr
ENST00000302326.4:c.3908C>A ENSP00000304956.4:p.Ser1303Tyr
ENST00000424656.1:c.261C>A
ENST00000497225.1:n.264C>A
NM_002430.2:c.3908C>A NP_002421.3:p.Ser1303Tyr
NM_002430.3:c.3908C>A MANE Select NP_002421.3:p.Ser1303Tyr
Search 100 bp 5'
Search 100 bp 3'