Canonical Allele Identifier: CA10343766
Gene: ANOS1 HGNC NCBI

Linked Data

dbSNP Id: rs752741795
gnomAD v2: X-8555855-G-A
gnomAD v4: X-8587814-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8587814G>A , CM000685.2:g.8587814G>A GRCh38
NC_000023.10:g.8555855G>A , CM000685.1:g.8555855G>A GRCh37
NC_000023.9:g.8515855G>A NCBI36
NG_007088.1:g.149373C>T
NG_007088.2:g.149373C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.706C>T MANE Select ENSP00000262648.3:p.His236Tyr
ENST00000262648.7:c.706C>T ENSP00000262648.3:p.His236Tyr
ENST00000619786.1:c.703C>T ENSP00000478734.1:p.His235Tyr
NM_000216.2:c.706C>T NP_000207.2:p.His236Tyr
XM_005274501.3:c.706C>T XP_005274558.1:p.His236Tyr
NM_000216.3:c.706C>T NP_000207.2:p.His236Tyr
XM_005274501.4:c.706C>T XP_005274558.1:p.His236Tyr
NM_000216.4:c.706C>T MANE Select NP_000207.2:p.His236Tyr