Canonical Allele Identifier: CA350677558
Gene: ZFAND2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219208308A>G , CM000664.2:g.219208308A>G GRCh38
NC_000002.11:g.220073030A>G , CM000664.1:g.220073030A>G GRCh37
NC_000002.10:g.219781274A>G NCBI36
NG_032110.1:g.15683T>C

Transcript Alleles

HGVS Amino-acid Change
NM_138802.3:c.487A>G MANE Select NP_620157.1:p.Ser163Gly
ENST00000289528.10:c.487A>G MANE Select ENSP00000289528.5:p.Ser163Gly
NM_001270998.1:c.487A>G NP_001257927.1:p.Ser163Gly
NM_001270998.2:c.487A>G NP_001257927.1:p.Ser163Gly
NM_001270999.1:c.355A>G NP_001257928.1:p.Ser119Gly
NM_001270999.2:c.355A>G NP_001257928.1:p.Ser119Gly
NM_138802.2:c.487A>G NP_620157.1:p.Ser163Gly
ENST00000289528.9:c.487A>G ENSP00000289528.5:p.Ser163Gly
ENST00000409097.5:c.487A>G ENSP00000387179.1:p.Ser163Gly
ENST00000409206.5:c.487A>G ENSP00000386824.1:p.Ser163Gly
ENST00000409217.5:c.487A>G ENSP00000386370.1:p.Ser163Gly
ENST00000409336.5:c.487A>G ENSP00000386898.1:p.Ser163Gly
ENST00000409594.5:c.487A>G ENSP00000386399.1:p.Ser163Gly
ENST00000422255.5:c.487A>G ENSP00000409931.1:p.Ser163Gly
ENST00000444522.6:c.487A>G ENSP00000411334.3:p.Ser163Gly
ENST00000448496.5:c.*191A>G ENSP00000388773.1:n.*191A>G
ENST00000464902.5:n.674A>G
ENST00000469596.5:n.389A>G
ENST00000475533.1:n.496A>G
ENST00000486734.5:n.407A>G
ENST00000621130.4:c.355A>G ENSP00000483320.1:p.Ser119Gly
XM_006712285.1:c.487A>G XP_006712348.1:p.Ser163Gly
XM_006712286.2:c.487A>G XP_006712349.1:p.Ser163Gly
XM_006712286.3:c.487A>G XP_006712349.1:p.Ser163Gly
XM_017003368.1:c.487A>G XP_016858857.1:p.Ser163Gly