Canonical Allele Identifier: CA2399817859

Gene: MN1

Linked Data

• dbSNP Id: rs1932753840

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27750469G>A , CM000684.2:g.27750469G>A	GRCh38
NC_000022.10:g.28146457G>A , CM000684.1:g.28146457G>A	GRCh37
NC_000022.9:g.26476457G>A	NCBI36
NG_023258.1:g.56030C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703102.1:n.934C>T
ENST00000302326.5:c.*446C>T MANE Select	ENSP00000304956.4:n.*446C>T
ENST00000302326.4:c.*446C>T	ENSP00000304956.4:n.*446C>T
ENST00000424656.1:c.456-241C>T
NM_002430.2:c.*446C>T	NP_002421.3:n.*446C>T
NM_002430.3:c.*446C>T MANE Select	NP_002421.3:n.*446C>T