Canonical Allele Identifier: CA66333326

Gene: PAX3

Linked Data

• dbSNP Id: rs76076975
• gnomAD v2: 2-223096614-G-T
• gnomAD v3: 2-222231895-G-T
• gnomAD v4: 2-222231895-G-T
• MyVariant Identifiers: chr2:g.223096614G>T (hg19) ; chr2:g.222231895G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222231895G>T , CM000664.2:g.222231895G>T	GRCh38
NC_000002.11:g.223096614G>T , CM000664.1:g.223096614G>T	GRCh37
NC_000002.10:g.222804858G>T	NCBI36
NG_011632.1:g.72087C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336840.11:c.792+183C>A	ENSP00000338767.5:n.792+183C>A
ENST00000344493.9:c.792+183C>A	ENSP00000342092.4:n.792+183C>A
ENST00000350526.9:c.792+183C>A	ENSP00000343052.4:n.792+183C>A
ENST00000392070.7:c.792+183C>A MANE Select	ENSP00000375922.3:n.792+183C>A
ENST00000646154.1:n.606+183C>A
ENST00000336840.10:c.792+183C>A	ENSP00000338767.5:n.792+183C>A
ENST00000344493.8:c.792+183C>A	ENSP00000342092.4:n.792+183C>A
ENST00000350526.8:c.792+183C>A	ENSP00000343052.4:n.792+183C>A
ENST00000392069.6:c.792+183C>A	ENSP00000375921.2:n.792+183C>A
ENST00000392070.6:c.792+183C>A	ENSP00000375922.2:n.792+183C>A
ENST00000409551.7:c.789+183C>A	ENSP00000386750.3:n.789+183C>A
NM_001127366.2:c.789+183C>A	NP_001120838.1:n.789+183C>A
NM_181457.3:c.792+183C>A	NP_852122.1:n.792+183C>A
NM_181458.3:c.792+183C>A	NP_852123.1:n.792+183C>A
NM_181459.3:c.792+183C>A	NP_852124.1:n.792+183C>A
NM_181460.3:c.792+183C>A	NP_852125.1:n.792+183C>A
NM_181461.3:c.792+183C>A	NP_852126.1:n.792+183C>A
XM_011511278.1:c.936+183C>A	XP_011509580.1:n.936+183C>A
XM_011511279.1:c.228+183C>A	XP_011509581.1:n.228+183C>A
XR_923945.1:n.287+9925G>T
XR_923946.1:n.288-117G>T
NM_001127366.3:c.789+183C>A	NP_001120838.1:n.789+183C>A
NM_181457.4:c.792+183C>A	NP_852122.1:n.792+183C>A
NM_181458.4:c.792+183C>A MANE Select	NP_852123.1:n.792+183C>A
NM_181459.4:c.792+183C>A	NP_852124.1:n.792+183C>A
NM_181460.4:c.792+183C>A	NP_852125.1:n.792+183C>A
NM_181461.4:c.792+183C>A	NP_852126.1:n.792+183C>A