Canonical Allele Identifier: CA6775003
Gene: ACACB HGNC NCBI

Linked Data

dbSNP Id: rs3742023

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109256177C>T , CM000674.2:g.109256177C>T GRCh38
NC_000012.11:g.109693982C>T , CM000674.1:g.109693982C>T GRCh37
NC_000012.10:g.108178365C>T NCBI36
NG_046907.1:g.149994C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338432.12:c.6204C>T MANE Select ENSP00000341044.7:p.His2068=
ENST00000338432.11:c.6204C>T ENSP00000341044.7:p.His2068=
ENST00000377848.7:c.6204C>T ENSP00000367079.3:p.His2068=
ENST00000377854.9:c.2202C>T ENSP00000367085.6:p.His734=
ENST00000538526.5:c.2203C>T
NM_001093.3:c.6204C>T NP_001084.3:p.His2068=
XM_005253876.3:c.6204C>T XP_005253933.1:p.His2068=
XM_006719365.2:c.6204C>T XP_006719428.1:p.His2068=
XM_006719367.2:c.5598C>T XP_006719430.1:p.His1866=
XM_011538259.1:c.6204C>T XP_011536561.1:p.His2068=
XM_011538260.1:c.6204C>T XP_011536562.1:p.His2068=
XM_011538261.1:c.6204C>T XP_011536563.1:p.His2068=
XM_011538262.1:c.6204C>T XP_011536564.1:p.His2068=
XM_011538263.1:c.6015C>T XP_011536565.1:p.His2005=
XM_011538264.1:c.5577C>T XP_011536566.1:p.His1859=
XR_944530.1:n.6951C>T
XR_944531.1:n.6951C>T
XR_944532.1:n.6951C>T
XM_005253876.4:c.6204C>T XP_005253933.1:p.His2068=
XM_006719367.4:c.5598C>T XP_006719430.1:p.His1866=
XM_011538259.2:c.6204C>T XP_011536561.1:p.His2068=
XM_011538263.3:c.6015C>T XP_011536565.1:p.His2005=
XM_011538264.3:c.5577C>T XP_011536566.1:p.His1859=
XM_017019252.2:c.5409C>T XP_016874741.1:p.His1803=
XR_002957320.1:n.6962C>T
XR_002957321.1:n.6864C>T
XR_002957322.1:n.5751C>T
XR_944530.2:n.6962C>T
XR_944532.3:n.6962C>T
NM_001093.4:c.6204C>T MANE Select NP_001084.3:p.His2068=