Canonical Allele Identifier: CA530851448

Gene: WDR35

Linked Data

• dbSNP Id: rs1364419027
• gnomAD v2: 2-20188909-G-A
• gnomAD v3: 2-19989148-G-A
• gnomAD v4: 2-19989148-G-A
• MyVariant Identifiers: chr2:g.20188909G>A (hg19) ; chr2:g.19989148G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989148G>A , CM000664.2:g.19989148G>A	GRCh38
NC_000002.11:g.20188909G>A , CM000664.1:g.20188909G>A	GRCh37
NC_000002.10:g.20052390G>A	NCBI36
NG_021212.1:g.5976C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.142+17C>T MANE Select	ENSP00000281405.5:n.142+17C>T
ENST00000345530.8:c.142+17C>T MANE Plus Clinical	ENSP00000314444.5:n.142+17C>T
ENST00000281405.8:c.142+17C>T	ENSP00000281405.4:n.142+17C>T
ENST00000345530.7:c.142+17C>T	ENSP00000314444.5:n.142+17C>T
ENST00000414212.5:c.142+17C>T	ENSP00000390802.1:n.142+17C>T
NM_001006657.1:c.142+17C>T	NP_001006658.1:n.142+17C>T
NM_020779.3:c.142+17C>T	NP_065830.2:n.142+17C>T
XR_426989.2:n.175+17C>T
XR_939699.1:n.175+17C>T
XR_001738862.1:n.175+17C>T
XR_426989.3:n.175+17C>T
XR_939699.3:n.175+17C>T
NM_001006657.2:c.142+17C>T MANE Plus Clinical	NP_001006658.1:n.142+17C>T
NM_020779.4:c.142+17C>T MANE Select	NP_065830.2:n.142+17C>T