Canonical Allele Identifier: CA1313503468
Gene: ZNF804A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184913615T= , CM000664.2:g.184913615T= GRCh38
NC_000002.11:g.185778342T= , CM000664.1:g.185778342T= GRCh37
NC_000002.10:g.185486587T= NCBI36
NG_046950.1:g.320250T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302277.7:c.256-19988T= MANE Select ENSP00000303252.6:n.256-19988T=
ENST00000302277.6:c.256-19988T= ENSP00000303252.6:n.256-19988T=
ENST00000613975.1:c.1-19988T= ENSP00000483032.1:n.1-19988T=
NM_194250.1:c.256-19988T= NP_919226.1:n.256-19988T=
NM_194250.2:c.256-19988T= MANE Select NP_919226.1:n.256-19988T=