Canonical Allele Identifier: CA1825813922
Gene: ZC3H3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143483735A>C , CM000670.2:g.143483735A>C GRCh38
NC_000008.10:g.144565905A>C , CM000670.1:g.144565905A>C GRCh37
NC_000008.9:g.144637048A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262577.6:c.1716-8150T>G MANE Select ENSP00000262577.5:n.1716-8150T>G
ENST00000262577.5:c.1716-8150T>G ENSP00000262577.5:n.1716-8150T>G
NM_015117.2:c.1716-8150T>G NP_055932.2:n.1716-8150T>G
XM_006716536.2:c.1902-8150T>G XP_006716599.2:n.1902-8150T>G
XM_011516943.1:c.1758-8150T>G XP_011515245.1:n.1758-8150T>G
XM_006716536.3:c.1902-8150T>G XP_006716599.2:n.1902-8150T>G
XM_011516943.2:c.1758-8150T>G XP_011515245.1:n.1758-8150T>G
XM_017013248.1:c.2100-8150T>G XP_016868737.1:n.2100-8150T>G
XM_017013249.1:c.2100-8150T>G XP_016868738.1:n.2100-8150T>G
NM_015117.3:c.1716-8150T>G MANE Select NP_055932.2:n.1716-8150T>G