Canonical Allele Identifier: CA411032943
Gene: MN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.28146952T>G (hg19) chr22:g.27750964T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750964T>G , CM000684.2:g.27750964T>G GRCh38
NC_000022.10:g.28146952T>G , CM000684.1:g.28146952T>G GRCh37
NC_000022.9:g.26476952T>G NCBI36
NG_023258.1:g.55535A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.439A>C
ENST00000302326.5:c.3914A>C MANE Select ENSP00000304956.4:p.His1305Pro
ENST00000302326.4:c.3914A>C ENSP00000304956.4:p.His1305Pro
ENST00000424656.1:c.267A>C
ENST00000497225.1:n.270A>C
NM_002430.2:c.3914A>C NP_002421.3:p.His1305Pro
NM_002430.3:c.3914A>C MANE Select NP_002421.3:p.His1305Pro
Search 100 bp 5'
Search 100 bp 3'