Canonical Allele Identifier: CA1095902696
Gene: ESR1 HGNC NCBI

Linked Data

dbSNP Id: rs1781873757

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151726701A>G , CM000668.2:g.151726701A>G GRCh38
NC_000006.11:g.152047836A>G , CM000668.1:g.152047836A>G GRCh37
NC_000006.10:g.152089529A>G NCBI36
NG_008493.1:g.41206A>G
NG_008493.2:g.75011A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000404742.5:c.-71+24696A>G ENSP00000385373.1:n.-71+24696A>G
ENST00000440973.5:c.-71+24696A>G ENSP00000405330.1:n.-71+24696A>G
ENST00000473497.5:n.204+24696A>G
NM_001122742.1:c.-71+24696A>G NP_001116214.1:n.-71+24696A>G
XM_006715374.2:c.-71+24696A>G XP_006715437.1:n.-71+24696A>G
XM_011535543.1:c.-185+24696A>G XP_011533845.1:n.-185+24696A>G
XM_011535547.1:c.-71+24696A>G XP_011533849.1:n.-71+24696A>G
XM_006715374.3:c.-71+24696A>G XP_006715437.1:n.-71+24696A>G
XM_011535543.2:c.-185+24696A>G XP_011533845.1:n.-185+24696A>G
XM_011535547.2:c.-71+24696A>G XP_011533849.1:n.-71+24696A>G
XM_017010376.1:c.-71+24696A>G XP_016865865.1:n.-71+24696A>G
XM_017010377.1:c.-71+24696A>G XP_016865866.1:n.-71+24696A>G
XM_017010378.1:c.-71+24696A>G XP_016865867.1:n.-71+24696A>G
XM_017010379.1:c.-71+24696A>G XP_016865868.1:n.-71+24696A>G
XM_017010380.1:c.-71+69938A>G XP_016865869.1:n.-71+69938A>G
XR_001743223.2:n.300+24696A>G
XR_002956266.1:n.300+24696A>G
NM_001122742.2:c.-71+24696A>G NP_001116214.1:n.-71+24696A>G
NM_001385568.1:c.-71+24696A>G NP_001372497.1:n.-71+24696A>G
NM_001385570.1:c.-71+24696A>G NP_001372499.1:n.-71+24696A>G