Canonical Allele Identifier: CA2399818049
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs989884543
gnomAD v4: 22-27750852-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750852G>C , CM000684.2:g.27750852G>C GRCh38
NC_000022.10:g.28146840G>C , CM000684.1:g.28146840G>C GRCh37
NC_000022.9:g.26476840G>C NCBI36
NG_023258.1:g.55647C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000703102.1:n.551C>G
ENST00000302326.5:c.*63C>G MANE Select ENSP00000304956.4:n.*63C>G
ENST00000302326.4:c.*63C>G ENSP00000304956.4:n.*63C>G
ENST00000424656.1:c.379C>G
ENST00000497225.1:n.382C>G
NM_002430.2:c.*63C>G NP_002421.3:n.*63C>G
NM_002430.3:c.*63C>G MANE Select NP_002421.3:n.*63C>G
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