Canonical Allele Identifier: CA12449724
Gene: ESR1 HGNC NCBI

Linked Data

dbSNP Id: rs1159327

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151726887C>T , CM000668.2:g.151726887C>T GRCh38
NC_000006.11:g.152048022C>T , CM000668.1:g.152048022C>T GRCh37
NC_000006.10:g.152089715C>T NCBI36
NG_008493.1:g.41392C>T
NG_008493.2:g.75197C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000404742.5:c.-71+24882C>T ENSP00000385373.1:p.=
ENST00000440973.5:c.-71+24882C>T ENSP00000405330.1:p.=
ENST00000473497.5:n.204+24882C>T
NM_001122742.1:c.-71+24882C>T NP_001116214.1:p.=
XM_006715374.2:c.-71+24882C>T XP_006715437.1:p.=
XM_011535543.1:c.-185+24882C>T XP_011533845.1:p.=
XM_011535547.1:c.-71+24882C>T XP_011533849.1:p.=
XM_006715374.3:c.-71+24882C>T XP_006715437.1:p.=
XM_011535543.2:c.-185+24882C>T XP_011533845.1:p.=
XM_011535547.2:c.-71+24882C>T XP_011533849.1:p.=
XM_017010376.1:c.-71+24882C>T XP_016865865.1:p.=
XM_017010377.1:c.-71+24882C>T XP_016865866.1:p.=
XM_017010378.1:c.-71+24882C>T XP_016865867.1:p.=
XM_017010379.1:c.-71+24882C>T XP_016865868.1:p.=
XM_017010380.1:c.-71+70124C>T XP_016865869.1:p.=
XR_001743223.2:n.300+24882C>T
XR_002956266.1:n.300+24882C>T
NM_001122742.2:c.-71+24882C>T NP_001116214.1:p.=
NM_001385568.1:c.-71+24882C>T NP_001372497.1:p.=
NM_001385570.1:c.-71+24882C>T NP_001372499.1:p.=