Canonical Allele Identifier: CA360613585
Gene: WDR36 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119086A>T , CM000667.2:g.111119086A>T GRCh38
NC_000005.9:g.110454784A>T , CM000667.1:g.110454784A>T GRCh37
NC_000005.8:g.110482683A>T NCBI36
NG_008979.1:g.31915A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1870A>T MANE Select ENSP00000424628.3:p.Thr624Ser
ENST00000506538.6:c.2038A>T ENSP00000423067.2:p.Thr680Ser
ENST00000513710.3:c.1870A>T ENSP00000424628.3:p.Thr624Ser
ENST00000612402.4:c.2038A>T ENSP00000479950.1:p.Thr680Ser
NM_139281.2:c.2038A>T NP_644810.1:p.Thr680Ser
XM_011543163.1:c.2038A>T XP_011541465.1:p.Thr680Ser
NM_139281.3:c.1870A>T MANE Select NP_644810.2:p.Thr624Ser