Canonical Allele Identifier: CA445744824
Gene: WDR36 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.110454738G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119040G>T , CM000667.2:g.111119040G>T GRCh38
NC_000005.9:g.110454738G>T , CM000667.1:g.110454738G>T GRCh37
NC_000005.8:g.110482637G>T NCBI36
NG_008979.1:g.31869G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1824G>T MANE Select ENSP00000424628.3:p.Ser608=
ENST00000506538.6:c.1992G>T ENSP00000423067.2:p.Ser664=
ENST00000513710.3:c.1824G>T ENSP00000424628.3:p.Ser608=
ENST00000612402.4:c.1992G>T ENSP00000479950.1:p.Ser664=
NM_139281.2:c.1992G>T NP_644810.1:p.Ser664=
XM_011543163.1:c.1992G>T XP_011541465.1:p.Ser664=
NM_139281.3:c.1824G>T MANE Select NP_644810.2:p.Ser608=