Canonical Allele Identifier: CA1313504181
Gene: ZNF804A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184915135T= , CM000664.2:g.184915135T= GRCh38
NC_000002.11:g.185779862T= , CM000664.1:g.185779862T= GRCh37
NC_000002.10:g.185488107T= NCBI36
NG_046950.1:g.321770T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-18468T= MANE Select ENSP00000303252.6:n.256-18468T=
ENST00000302277.6:c.256-18468T= ENSP00000303252.6:n.256-18468T=
ENST00000613975.1:c.1-18468T= ENSP00000483032.1:n.1-18468T=
NM_194250.1:c.256-18468T= NP_919226.1:n.256-18468T=
NM_194250.2:c.256-18468T= MANE Select NP_919226.1:n.256-18468T=