Canonical Allele Identifier: CA2147904019
Gene: ESRRB HGNC NCBI

Linked Data

dbSNP Id: rs1223062127
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.76371327C>G , CM000676.2:g.76371327C>G GRCh38
NC_000014.8:g.76837670C>G , CM000676.1:g.76837670C>G GRCh37
NC_000014.7:g.75907423C>G NCBI36
NG_012278.1:g.4981C>G
NG_012278.2:g.4981C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000512784.6:c.2+60411C>G ENSP00000424992.2:n.2+60411C>G
ENST00000505752.5:c.-391C>G ENSP00000423004.1:n.-391C>G
ENST00000512784.5:c.2+60411C>G ENSP00000424992.1:n.2+60411C>G
XM_011536548.1:c.-391C>G XP_011534850.1:n.-391C>G
NM_004452.4:c.-391C>G NP_004443.3:n.-391C>G
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