Canonical Allele Identifier: CA14644995
Gene: ZC3H4 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.47065746G>A
GRCh37 chr19:g.47569003G>A
gnomAD v2:
19:47569003 G / A
gnomAD v3:
19:47065746 G / A
gnomAD v4:
chr19-47065746-G-A
Joint Max Group AF 0.67018418 (NFE)
Genomes Max Group AF 0.67024818 (NFE)
Exomes Max Group AF 0.57852093 (NFE)
dbSNP:
3810291
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47065746G>A , CM000681.2:g.47065746G>A GRCh38
NC_000019.9:g.47569003G>A , CM000681.1:g.47569003G>A GRCh37
NC_000019.8:g.52260843G>A NCBI36
NG_027798.1:g.53007C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253048.10:c.*610C>T MANE Select ENSP00000253048.4:n.*610C>T
ENST00000253048.9:c.*610C>T ENSP00000253048.4:n.*610C>T
ENST00000594019.5:n.2372C>T
ENST00000601973.1:c.3341C>T
NM_015168.1:c.*610C>T NP_055983.1:n.*610C>T
XM_005258676.2:c.*610C>T XP_005258733.1:n.*610C>T
XM_005258677.3:c.*610C>T XP_005258734.1:n.*610C>T
XM_005258678.1:c.*610C>T XP_005258735.1:n.*610C>T
XM_006723113.2:c.*610C>T XP_006723176.1:n.*610C>T
XM_011526668.1:c.*610C>T XP_011524970.1:n.*610C>T
XM_011526669.1:c.*610C>T XP_011524971.1:n.*610C>T
XM_011526670.1:c.*610C>T XP_011524972.1:n.*610C>T
XM_011526671.1:c.*610C>T XP_011524973.1:n.*610C>T
XM_017026530.2:c.*610C>T XP_016882019.1:n.*610C>T
XM_017026531.1:c.*610C>T XP_016882020.1:n.*610C>T
NM_015168.2:c.*610C>T MANE Select NP_055983.1:n.*610C>T
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