Canonical Allele Identifier: CA199051406

Gene: ASTN2

Linked Data

• dbSNP Id: rs72750057
• gnomAD v2: 9-119544435-A-T
• gnomAD v3: 9-116782156-A-T
• gnomAD v4: 9-116782156-A-T
• MyVariant Identifiers: chr9:g.119544435A>T (hg19) ; chr9:g.116782156A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.116782156A>T , CM000671.2:g.116782156A>T	GRCh38
NC_000009.11:g.119544435A>T , CM000671.1:g.119544435A>T	GRCh37
NC_000009.10:g.118584256A>T	NCBI36
NG_021409.1:g.637883T>A
NG_021409.2:g.637902T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313400.9:c.2396+23476T>A MANE Select	ENSP00000314038.4:n.2396+23476T>A
ENST00000361477.8:c.2243+23476T>A	ENSP00000355116.5:n.2243+23476T>A
ENST00000313400.8:c.2396+23476T>A	ENSP00000314038.4:n.2396+23476T>A
ENST00000361209.6:c.2243+23476T>A	ENSP00000354504.2:n.2243+23476T>A
ENST00000361477.7:c.-449+23476T>A	ENSP00000355116.4:n.-449+23476T>A
ENST00000373986.7:c.1565+23476T>A	ENSP00000363098.3:n.1565+23476T>A
NM_014010.4:c.2243+23476T>A	NP_054729.3:n.2243+23476T>A
NM_001365068.1:c.2396+23476T>A MANE Select	NP_001351997.1:n.2396+23476T>A
NM_001365069.1:c.2384+23476T>A	NP_001351998.1:n.2384+23476T>A
NM_014010.5:c.2243+23476T>A	NP_054729.3:n.2243+23476T>A