Canonical Allele Identifier: CA763233165

Gene: WDR35

Linked Data

• dbSNP Id: rs1378712382
• MyVariant Identifiers: chr2:g.20188837T>G (hg19) ; chr2:g.19989076T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989076T>G , CM000664.2:g.19989076T>G	GRCh38
NC_000002.11:g.20188837T>G , CM000664.1:g.20188837T>G	GRCh37
NC_000002.10:g.20052318T>G	NCBI36
NG_021212.1:g.6048A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.142+89A>C MANE Select	ENSP00000281405.5:n.142+89A>C
ENST00000345530.8:c.142+89A>C MANE Plus Clinical	ENSP00000314444.5:n.142+89A>C
ENST00000281405.8:c.142+89A>C	ENSP00000281405.4:n.142+89A>C
ENST00000345530.7:c.142+89A>C	ENSP00000314444.5:n.142+89A>C
ENST00000414212.5:c.142+89A>C	ENSP00000390802.1:n.142+89A>C
NM_001006657.1:c.142+89A>C	NP_001006658.1:n.142+89A>C
NM_020779.3:c.142+89A>C	NP_065830.2:n.142+89A>C
XR_426989.2:n.175+89A>C
XR_939699.1:n.175+89A>C
XR_001738862.1:n.175+89A>C
XR_426989.3:n.175+89A>C
XR_939699.3:n.175+89A>C
NM_001006657.2:c.142+89A>C MANE Plus Clinical	NP_001006658.1:n.142+89A>C
NM_020779.4:c.142+89A>C MANE Select	NP_065830.2:n.142+89A>C