Canonical Allele Identifier: CA2818640090
Gene: MN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750869A>C , CM000684.2:g.27750869A>C GRCh38
NC_000022.10:g.28146857A>C , CM000684.1:g.28146857A>C GRCh37
NC_000022.9:g.26476857A>C NCBI36
NG_023258.1:g.55630T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.534T>G
ENST00000302326.5:c.*46T>G MANE Select ENSP00000304956.4:n.*46T>G
ENST00000302326.4:c.*46T>G ENSP00000304956.4:n.*46T>G
ENST00000424656.1:c.362T>G
ENST00000497225.1:n.365T>G
NM_002430.2:c.*46T>G NP_002421.3:n.*46T>G
NM_002430.3:c.*46T>G MANE Select NP_002421.3:n.*46T>G
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Search 100 bp 3'