Canonical Allele Identifier: CA411033636
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27751057-G-C
MyVariant Identifiers: chr22:g.28147045G>C (hg19) chr22:g.27751057G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27751057G>C , CM000684.2:g.27751057G>C GRCh38
NC_000022.10:g.28147045G>C , CM000684.1:g.28147045G>C GRCh37
NC_000022.9:g.26477045G>C NCBI36
NG_023258.1:g.55442C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.346C>G
ENST00000302326.5:c.3821C>G MANE Select ENSP00000304956.4:p.Pro1274Arg
ENST00000302326.4:c.3821C>G ENSP00000304956.4:p.Pro1274Arg
ENST00000424656.1:c.174C>G
ENST00000497225.1:n.177C>G
NM_002430.2:c.3821C>G NP_002421.3:p.Pro1274Arg
NM_002430.3:c.3821C>G MANE Select NP_002421.3:p.Pro1274Arg
Search 100 bp 5'
Search 100 bp 3'