Canonical Allele Identifier: CA345846745
Gene: GREB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11587390A>G , CM000664.2:g.11587390A>G GRCh38
NC_000002.11:g.11727516A>G , CM000664.1:g.11727516A>G GRCh37
NC_000002.10:g.11644967A>G NCBI36
NG_029429.1:g.58275A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000381486.7:c.1160-1356A>G MANE Select ENSP00000370896.2:n.1160-1356A>G
ENST00000234142.9:c.1160-1356A>G ENSP00000234142.5:n.1160-1356A>G
ENST00000263834.9:c.1168A>G ENSP00000263834.5:p.Asn390Asp
ENST00000381483.6:c.1160-1356A>G ENSP00000370892.2:n.1160-1356A>G
ENST00000381486.6:c.1160-1356A>G ENSP00000370896.2:n.1160-1356A>G
NM_014668.3:c.1160-1356A>G NP_055483.2:n.1160-1356A>G
NM_033090.2:c.1160-1356A>G NP_149081.1:n.1160-1356A>G
NM_148903.2:c.1168A>G NP_683701.2:p.Asn390Asp
XM_005246192.3:c.1160-1356A>G XP_005246249.1:n.1160-1356A>G
XM_011510418.1:c.1160-1356A>G XP_011508720.1:n.1160-1356A>G
XM_011510419.1:c.1160-1356A>G XP_011508721.1:n.1160-1356A>G
XM_011510420.1:c.1160-1356A>G XP_011508722.1:n.1160-1356A>G
XM_011510421.1:c.1160-1356A>G XP_011508723.1:n.1160-1356A>G
XM_011510423.1:c.1160-1356A>G XP_011508725.1:n.1160-1356A>G
XR_922686.1:n.1321-1356A>G
XM_005246192.4:c.1160-1356A>G XP_005246249.1:n.1160-1356A>G
XM_011510418.3:c.1160-1356A>G XP_011508720.1:n.1160-1356A>G
XM_011510419.3:c.1160-1356A>G XP_011508721.1:n.1160-1356A>G
XM_011510423.3:c.1160-1356A>G XP_011508725.1:n.1160-1356A>G
XM_024453250.1:c.1160-1356A>G XP_024309018.1:n.1160-1356A>G
XM_024453251.1:c.1160-1356A>G XP_024309019.1:n.1160-1356A>G
XM_024453252.1:c.1160-1356A>G XP_024309020.1:n.1160-1356A>G
XM_024453253.1:c.1160-1356A>G XP_024309021.1:n.1160-1356A>G
XM_024453254.1:c.1160-1356A>G XP_024309022.1:n.1160-1356A>G
XM_024453255.1:c.1160-1356A>G XP_024309023.1:n.1160-1356A>G
XM_024453256.1:c.1160-1356A>G XP_024309024.1:n.1160-1356A>G
XR_001739081.2:n.2090-1356A>G
XR_922686.3:n.2089-1356A>G
NM_014668.4:c.1160-1356A>G MANE Select NP_055483.2:n.1160-1356A>G
NM_033090.3:c.1160-1356A>G NP_149081.1:n.1160-1356A>G
NM_148903.3:c.1168A>G NP_683701.2:p.Asn390Asp