Canonical Allele Identifier: CA322870706
Gene: MN1 HGNC NCBI

Linked Data

dbSNP Id: rs989884543

Genomic Alleles

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

Transcript Alleles

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