Canonical Allele Identifier: CA390479104
Gene: ESRRB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76491593T>G , CM000676.2:g.76491593T>G GRCh38
NC_000014.8:g.76957936T>G , CM000676.1:g.76957936T>G GRCh37
NC_000014.7:g.76027689T>G NCBI36
NG_012278.1:g.125247T>G
NG_012278.2:g.125247T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000380887.7:c.934T>G ENSP00000370270.2:p.Ser312Ala
ENST00000505752.6:c.934T>G ENSP00000423004.1:p.Ser312Ala
ENST00000512784.6:c.949T>G ENSP00000424992.2:p.Ser317Ala
ENST00000644823.1:c.997T>G MANE Select ENSP00000493776.1:p.Ser333Ala
ENST00000380887.6:c.934T>G ENSP00000370270.2:p.Ser312Ala
ENST00000505752.5:c.934T>G ENSP00000423004.1:p.Ser312Ala
ENST00000509242.5:c.934T>G ENSP00000422488.1:p.Ser312Ala
ENST00000512784.5:c.949T>G ENSP00000424992.1:p.Ser317Ala
ENST00000556177.1:c.934T>G ENSP00000451658.1:p.Ser312Ala
NM_004452.3:c.934T>G NP_004443.3:p.Ser312Ala
XM_005267404.2:c.997T>G XP_005267461.1:p.Ser333Ala
XM_011536547.1:c.997T>G XP_011534849.1:p.Ser333Ala
XM_011536548.1:c.934T>G XP_011534850.1:p.Ser312Ala
XM_011536549.1:c.934T>G XP_011534851.1:p.Ser312Ala
XM_011536550.1:c.934T>G XP_011534852.1:p.Ser312Ala
XM_011536551.1:c.934T>G XP_011534853.1:p.Ser312Ala
XM_011536552.1:c.934T>G XP_011534854.1:p.Ser312Ala
XM_011536553.1:c.997T>G XP_011534855.1:p.Ser333Ala
XM_011536554.1:c.997T>G XP_011534856.1:p.Ser333Ala
XM_011536555.1:c.256T>G XP_011534857.1:p.Ser86Ala
XR_943401.1:n.1244T>G
XR_944039.1:n.144+10564A>C
XM_011536547.2:c.997T>G XP_011534849.1:p.Ser333Ala
XM_011536550.2:c.934T>G XP_011534852.1:p.Ser312Ala
XM_011536553.2:c.997T>G XP_011534855.1:p.Ser333Ala
XM_011536554.2:c.997T>G XP_011534856.1:p.Ser333Ala
XM_017021085.1:c.934T>G XP_016876574.1:p.Ser312Ala
XM_024449508.1:c.997T>G XP_024305276.1:p.Ser333Ala
XM_024449509.1:c.934T>G XP_024305277.1:p.Ser312Ala
XR_001750189.1:n.1467T>G
XR_943401.2:n.1467T>G
NM_001379180.1:c.997T>G MANE Select NP_001366109.1:p.Ser333Ala
NM_004452.4:c.934T>G NP_004443.3:p.Ser312Ala