Canonical Allele Identifier: CA1024815651
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs1158099520
gnomAD v3: 22-27750864-C-T
gnomAD v4: 22-27750864-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750864C>T , CM000684.2:g.27750864C>T GRCh38
NC_000022.10:g.28146852C>T , CM000684.1:g.28146852C>T GRCh37
NC_000022.9:g.26476852C>T NCBI36
NG_023258.1:g.55635G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.539G>A
ENST00000302326.5:c.*51G>A MANE Select ENSP00000304956.4:n.*51G>A
ENST00000302326.4:c.*51G>A ENSP00000304956.4:n.*51G>A
ENST00000424656.1:c.367G>A
ENST00000497225.1:n.370G>A
NM_002430.2:c.*51G>A NP_002421.3:n.*51G>A
NM_002430.3:c.*51G>A MANE Select NP_002421.3:n.*51G>A
Search 100 bp 5'
Search 100 bp 3'