Canonical Allele Identifier: CA360613489
Gene: WDR36 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119038T>C , CM000667.2:g.111119038T>C GRCh38
NC_000005.9:g.110454736T>C , CM000667.1:g.110454736T>C GRCh37
NC_000005.8:g.110482635T>C NCBI36
NG_008979.1:g.31867T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1822T>C MANE Select ENSP00000424628.3:p.Ser608Pro
ENST00000506538.6:c.1990T>C ENSP00000423067.2:p.Ser664Pro
ENST00000513710.3:c.1822T>C ENSP00000424628.3:p.Ser608Pro
ENST00000612402.4:c.1990T>C ENSP00000479950.1:p.Ser664Pro
NM_139281.2:c.1990T>C NP_644810.1:p.Ser664Pro
XM_011543163.1:c.1990T>C XP_011541465.1:p.Ser664Pro
NM_139281.3:c.1822T>C MANE Select NP_644810.2:p.Ser608Pro