Canonical Allele Identifier: CA638787370
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs1359984523
gnomAD v2: 22-28146856-C-T
gnomAD v4: 22-27750868-C-T
MyVariant Identifiers: chr22:g.28146856C>T (hg19) chr22:g.27750868C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750868C>T , CM000684.2:g.27750868C>T GRCh38
NC_000022.10:g.28146856C>T , CM000684.1:g.28146856C>T GRCh37
NC_000022.9:g.26476856C>T NCBI36
NG_023258.1:g.55631G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.535G>A
ENST00000302326.5:c.*47G>A MANE Select ENSP00000304956.4:n.*47G>A
ENST00000302326.4:c.*47G>A ENSP00000304956.4:n.*47G>A
ENST00000424656.1:c.363G>A
ENST00000497225.1:n.366G>A
NM_002430.2:c.*47G>A NP_002421.3:n.*47G>A
NM_002430.3:c.*47G>A MANE Select NP_002421.3:n.*47G>A
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