Canonical Allele Identifier: CA1024815644
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs1601319385
gnomAD v3: 22-27750849-T-G
gnomAD v4: 22-27750849-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750849T>G , CM000684.2:g.27750849T>G GRCh38
NC_000022.10:g.28146837T>G , CM000684.1:g.28146837T>G GRCh37
NC_000022.9:g.26476837T>G NCBI36
NG_023258.1:g.55650A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.554A>C
ENST00000302326.5:c.*66A>C MANE Select ENSP00000304956.4:n.*66A>C
ENST00000302326.4:c.*66A>C ENSP00000304956.4:n.*66A>C
ENST00000424656.1:c.382A>C
ENST00000497225.1:n.385A>C
NM_002430.2:c.*66A>C NP_002421.3:n.*66A>C
NM_002430.3:c.*66A>C MANE Select NP_002421.3:n.*66A>C
Search 100 bp 5'
Search 100 bp 3'