Canonical Allele Identifier: CA2535379726
Gene: WDR36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119330A>C , CM000667.2:g.111119330A>C GRCh38
NC_000005.9:g.110455028A>C , CM000667.1:g.110455028A>C GRCh37
NC_000005.8:g.110482927A>C NCBI36
NG_008979.1:g.32159A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1904+210A>C MANE Select ENSP00000424628.3:n.1904+210A>C
ENST00000506538.6:c.2072+210A>C ENSP00000423067.2:n.2072+210A>C
ENST00000513710.3:c.1904+210A>C ENSP00000424628.3:n.1904+210A>C
ENST00000612402.4:c.2072+210A>C ENSP00000479950.1:n.2072+210A>C
NM_139281.2:c.2072+210A>C NP_644810.1:n.2072+210A>C
XM_011543163.1:c.2072+210A>C XP_011541465.1:n.2072+210A>C
NM_139281.3:c.1904+210A>C MANE Select NP_644810.2:n.1904+210A>C