Canonical Allele Identifier: CA411033265
Gene: MN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.28146988T>G (hg19) chr22:g.27751000T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27751000T>G , CM000684.2:g.27751000T>G GRCh38
NC_000022.10:g.28146988T>G , CM000684.1:g.28146988T>G GRCh37
NC_000022.9:g.26476988T>G NCBI36
NG_023258.1:g.55499A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.403A>C
ENST00000302326.5:c.3878A>C MANE Select ENSP00000304956.4:p.Lys1293Thr
ENST00000302326.4:c.3878A>C ENSP00000304956.4:p.Lys1293Thr
ENST00000424656.1:c.231A>C
ENST00000497225.1:n.234A>C
NM_002430.2:c.3878A>C NP_002421.3:p.Lys1293Thr
NM_002430.3:c.3878A>C MANE Select NP_002421.3:p.Lys1293Thr
Search 100 bp 5'
Search 100 bp 3'