Canonical Allele Identifier: CA1874916066

Gene: ASTN2

Linked Data

• dbSNP Id: rs1588288576

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.116782071G>T , CM000671.2:g.116782071G>T	GRCh38
NC_000009.11:g.119544350G>T , CM000671.1:g.119544350G>T	GRCh37
NC_000009.10:g.118584171G>T	NCBI36
NG_021409.1:g.637968C>A
NG_021409.2:g.637987C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000313400.9:c.2396+23561C>A MANE Select	ENSP00000314038.4:n.2396+23561C>A
ENST00000361477.8:c.2243+23561C>A	ENSP00000355116.5:n.2243+23561C>A
ENST00000313400.8:c.2396+23561C>A	ENSP00000314038.4:n.2396+23561C>A
ENST00000361209.6:c.2243+23561C>A	ENSP00000354504.2:n.2243+23561C>A
ENST00000361477.7:c.-449+23561C>A	ENSP00000355116.4:n.-449+23561C>A
ENST00000373986.7:c.1565+23561C>A	ENSP00000363098.3:n.1565+23561C>A
NM_014010.4:c.2243+23561C>A	NP_054729.3:n.2243+23561C>A
NM_001365068.1:c.2396+23561C>A MANE Select	NP_001351997.1:n.2396+23561C>A
NM_001365069.1:c.2384+23561C>A	NP_001351998.1:n.2384+23561C>A
NM_014010.5:c.2243+23561C>A	NP_054729.3:n.2243+23561C>A