Canonical Allele Identifier: CA411032932
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750962-A-G
MyVariant Identifiers: chr22:g.28146950A>G (hg19) chr22:g.27750962A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750962A>G , CM000684.2:g.27750962A>G GRCh38
NC_000022.10:g.28146950A>G , CM000684.1:g.28146950A>G GRCh37
NC_000022.9:g.26476950A>G NCBI36
NG_023258.1:g.55537T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.441T>C
ENST00000302326.5:c.3916T>C MANE Select ENSP00000304956.4:p.Ser1306Pro
ENST00000302326.4:c.3916T>C ENSP00000304956.4:p.Ser1306Pro
ENST00000424656.1:c.269T>C
ENST00000497225.1:n.272T>C
NM_002430.2:c.3916T>C NP_002421.3:p.Ser1306Pro
NM_002430.3:c.3916T>C MANE Select NP_002421.3:p.Ser1306Pro
Search 100 bp 5'
Search 100 bp 3'