Canonical Allele Identifier: CA1313503466
Gene: ZNF804A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.184913614G= , CM000664.2:g.184913614G= GRCh38
NC_000002.11:g.185778341G= , CM000664.1:g.185778341G= GRCh37
NC_000002.10:g.185486586G= NCBI36
NG_046950.1:g.320249G=

Transcript Alleles

HGVS Amino-acid change
ENST00000302277.7:c.256-19989G= MANE Select ENSP00000303252.6:n.256-19989G=
ENST00000302277.6:c.256-19989G= ENSP00000303252.6:n.256-19989G=
ENST00000613975.1:c.1-19989G= ENSP00000483032.1:n.1-19989G=
NM_194250.1:c.256-19989G= NP_919226.1:n.256-19989G=
NM_194250.2:c.256-19989G= MANE Select NP_919226.1:n.256-19989G=