Canonical Allele Identifier: CA594030970
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1231469265

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62501470A>G , CM000672.2:g.62501470A>G GRCh38
NC_000010.10:g.64261229A>G , CM000672.1:g.64261229A>G GRCh37
NC_000010.9:g.63931235A>G NCBI36
NG_021209.1:g.132314A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+41673A>G ENSP00000502188.1:n.981+41673A>G
ENST00000410046.7:c.981+41673A>G ENSP00000387091.3:n.981+41673A>G
NM_199451.2:c.981+41673A>G NP_955523.1:n.981+41673A>G
XM_017015937.2:c.981+41673A>G XP_016871426.1:n.981+41673A>G
NM_199451.3:c.981+41673A>G NP_955523.1:n.981+41673A>G