Canonical Allele Identifier: CA1095902721
Gene: ESR1 HGNC NCBI

Linked Data

dbSNP Id: rs1781878567

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151726774G>C , CM000668.2:g.151726774G>C GRCh38
NC_000006.11:g.152047909G>C , CM000668.1:g.152047909G>C GRCh37
NC_000006.10:g.152089602G>C NCBI36
NG_008493.1:g.41279G>C
NG_008493.2:g.75084G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000404742.5:c.-71+24769G>C ENSP00000385373.1:n.-71+24769G>C
ENST00000440973.5:c.-71+24769G>C ENSP00000405330.1:n.-71+24769G>C
ENST00000473497.5:n.204+24769G>C
NM_001122742.1:c.-71+24769G>C NP_001116214.1:n.-71+24769G>C
XM_006715374.2:c.-71+24769G>C XP_006715437.1:n.-71+24769G>C
XM_011535543.1:c.-185+24769G>C XP_011533845.1:n.-185+24769G>C
XM_011535547.1:c.-71+24769G>C XP_011533849.1:n.-71+24769G>C
XM_006715374.3:c.-71+24769G>C XP_006715437.1:n.-71+24769G>C
XM_011535543.2:c.-185+24769G>C XP_011533845.1:n.-185+24769G>C
XM_011535547.2:c.-71+24769G>C XP_011533849.1:n.-71+24769G>C
XM_017010376.1:c.-71+24769G>C XP_016865865.1:n.-71+24769G>C
XM_017010377.1:c.-71+24769G>C XP_016865866.1:n.-71+24769G>C
XM_017010378.1:c.-71+24769G>C XP_016865867.1:n.-71+24769G>C
XM_017010379.1:c.-71+24769G>C XP_016865868.1:n.-71+24769G>C
XM_017010380.1:c.-71+70011G>C XP_016865869.1:n.-71+70011G>C
XR_001743223.2:n.300+24769G>C
XR_002956266.1:n.300+24769G>C
NM_001122742.2:c.-71+24769G>C NP_001116214.1:n.-71+24769G>C
NM_001385568.1:c.-71+24769G>C NP_001372497.1:n.-71+24769G>C
NM_001385570.1:c.-71+24769G>C NP_001372499.1:n.-71+24769G>C