Canonical Allele Identifier: CA14758655
Gene: EYA2 HGNC NCBI

Linked Data

dbSNP Id: rs878131

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.47051863A>G , CM000682.2:g.47051863A>G GRCh38
NC_000020.10:g.45680502A>G , CM000682.1:g.45680502A>G GRCh37
NC_000020.9:g.45113909A>G NCBI36
NG_011673.1:g.161994A>G
NG_011673.2:g.161994A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000327619.10:c.416-20322A>G MANE Select ENSP00000333640.5:n.416-20322A>G
ENST00000317304.10:c.416-20322A>G ENSP00000321590.6:n.416-20322A>G
ENST00000327619.9:c.416-20322A>G ENSP00000333640.5:n.416-20322A>G
ENST00000357410.7:c.416-20322A>G ENSP00000349986.3:n.416-20322A>G
ENST00000458636.2:c.274+35566A>G ENSP00000395427.1:n.274+35566A>G
ENST00000497062.6:c.344-20322A>G ENSP00000417105.3:n.344-20322A>G
ENST00000611592.4:c.416-20322A>G ENSP00000483392.1:n.416-20322A>G
NM_005244.4:c.416-20322A>G NP_005235.3:n.416-20322A>G
NM_172110.3:c.416-20322A>G NP_742108.2:n.416-20322A>G
XM_005260327.1:c.415+35566A>G XP_005260384.1:n.415+35566A>G
XM_011528687.1:c.416-20322A>G XP_011526989.1:n.416-20322A>G
XM_005260327.2:c.415+35566A>G XP_005260384.1:n.415+35566A>G
XM_017027721.2:c.416-20322A>G XP_016883210.1:n.416-20322A>G
NM_005244.5:c.416-20322A>G MANE Select NP_005235.3:n.416-20322A>G
NM_172110.4:c.416-20322A>G NP_742108.2:n.416-20322A>G