Canonical Allele Identifier: CA64076370
Gene: WDR12 HGNC NCBI

Linked Data

dbSNP Id: rs6725887

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202881162T>C , CM000664.2:g.202881162T>C GRCh38
NC_000002.11:g.203745885T>C , CM000664.1:g.203745885T>C GRCh37
NC_000002.10:g.203454130T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000688520.1:c.1195-225A>G ENSP00000509107.1:n.1195-225A>G
ENST00000261015.5:c.1195-225A>G MANE Select ENSP00000261015.4:n.1195-225A>G
ENST00000261015.4:c.1195-225A>G ENSP00000261015.3:n.1195-225A>G
ENST00000467777.1:n.146-225A>G
NM_018256.3:c.1195-225A>G NP_060726.3:n.1195-225A>G
XM_011511469.1:c.781-225A>G XP_011509771.1:n.781-225A>G
XM_011511469.3:c.781-225A>G XP_011509771.1:n.781-225A>G
NM_001371664.1:c.781-225A>G NP_001358593.1:n.781-225A>G
NM_018256.4:c.1195-225A>G MANE Select NP_060726.3:n.1195-225A>G