Canonical Allele Identifier: CA199042469
Gene: ASTN2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10983238

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.116571404C>A , CM000671.2:g.116571404C>A GRCh38
NC_000009.10:g.118373504C>A NCBI36
NC_000009.11:g.119333683C>A , CM000671.1:g.119333683C>A GRCh37
NG_021409.1:g.848635G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000288520.9:c.658+46920G>T ENSP00000288520.5:p.=
ENST00000313400.8:c.3355+46920G>T ENSP00000314038.4:p.=
ENST00000341734.8:c.511+46920G>T ENSP00000339925.4:p.=
ENST00000361209.6:c.3202+46920G>T ENSP00000354504.2:p.=
ENST00000361477.7:c.511+46920G>T ENSP00000355116.4:p.=
ENST00000373986.7:n.2524+46920G>T ENSP00000363098.3:p.=
NM_001184734.1:c.511+46920G>T NP_001171663.1:p.=
NM_014010.4:c.3202+46920G>T NP_054729.3:p.=
NM_198186.3:c.658+46920G>T NP_937829.3:p.=
NM_198187.3:c.511+46920G>T NP_937830.3:p.=
NM_198188.2:c.511+46920G>T NP_937831.1:p.=