Canonical Allele Identifier: CA87818401

Gene: WDR49

Linked Data

• dbSNP Id: rs77627676
• gnomAD v3: 3-167630990-C-T
• gnomAD v4: 3-167630990-C-T
• MyVariant Identifiers: chr3:g.167348778C>T (hg19) ; chr3:g.167630990C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.167630990C>T , CM000665.2:g.167630990C>T	GRCh38
NC_000003.11:g.167348778C>T , CM000665.1:g.167348778C>T	GRCh37
NC_000003.10:g.168831472C>T	NCBI36
NG_053014.1:g.32014G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647816.2:c.166-3698G>A	ENSP00000497120.1:n.166-3698G>A
ENST00000682715.1:c.166-3698G>A MANE Select	ENSP00000507497.1:n.166-3698G>A
ENST00000647816.1:c.166-3698G>A	ENSP00000497120.1:n.166-3698G>A
ENST00000308378.7:c.-66+22271G>A	ENSP00000311343.3:n.-66+22271G>A
ENST00000460448.5:c.165+22271G>A	ENSP00000417090.1:n.165+22271G>A
ENST00000466760.5:c.165+22271G>A	ENSP00000418718.1:n.165+22271G>A
ENST00000471198.1:n.410+2419G>A
ENST00000479765.5:c.166-3698G>A	ENSP00000419749.1:n.166-3698G>A
ENST00000488012.5:c.166-9347G>A	ENSP00000419917.1:n.166-9347G>A
NM_178824.3:c.-66+22271G>A	NP_849146.1:n.-66+22271G>A
NM_001348951.1:c.166-3698G>A	NP_001335880.1:n.166-3698G>A
NM_001348952.1:c.166-3698G>A	NP_001335881.1:n.166-3698G>A
NM_001366157.1:c.166-3698G>A MANE Select	NP_001353086.1:n.166-3698G>A
NM_001366158.1:c.-66+22271G>A	NP_001353087.1:n.-66+22271G>A
NM_001348951.2:c.166-3698G>A	NP_001335880.1:n.166-3698G>A
NM_001348952.2:c.166-3698G>A	NP_001335881.1:n.166-3698G>A