Canonical Allele Identifier: CA10165936
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs761957381

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750969G>C , CM000684.2:g.27750969G>C GRCh38
NC_000022.10:g.28146957G>C , CM000684.1:g.28146957G>C GRCh37
NC_000022.9:g.26476957G>C NCBI36
NG_023258.1:g.55530C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.434C>G
ENST00000302326.5:c.3909C>G MANE Select ENSP00000304956.4:p.Ser1303=
ENST00000302326.4:c.3909C>G ENSP00000304956.4:p.Ser1303=
ENST00000424656.1:c.262C>G
ENST00000497225.1:n.265C>G
NM_002430.2:c.3909C>G NP_002421.3:p.Ser1303=
NM_002430.3:c.3909C>G MANE Select NP_002421.3:p.Ser1303=