Canonical Allele Identifier: CA1825841179
Gene: ZC3H3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143538013T= , CM000670.2:g.143538013T= GRCh38
NC_000008.10:g.144620183T= , CM000670.1:g.144620183T= GRCh37
NC_000008.9:g.144691326T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_015117.3:c.1354A= MANE Select NP_055932.2:p.Ser452=
ENST00000262577.6:c.1354A= MANE Select ENSP00000262577.5:p.Ser452=
NM_015117.2:c.1354A= NP_055932.2:p.Ser452=
ENST00000262577.5:c.1354A= ENSP00000262577.5:p.Ser452=
XM_006716536.2:c.1540A= XP_006716599.2:p.Ser514=
XM_006716536.3:c.1540A= XP_006716599.2:p.Ser514=
XM_011516943.1:c.1396A= XP_011515245.1:p.Ser466=
XM_011516943.2:c.1396A= XP_011515245.1:p.Ser466=
XM_011516944.1:c.1396A= XP_011515246.1:p.Ser466=
XM_011516944.2:c.1396A= XP_011515246.1:p.Ser466=
XM_017013248.1:c.1738A= XP_016868737.1:p.Ser580=
XM_017013249.1:c.1738A= XP_016868738.1:p.Ser580=
XR_928313.1:n.1484A=
XR_928313.3:n.1498A=