Canonical Allele Identifier: CA12919493

Gene: ZC3H3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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