Canonical Allele Identifier: CA1474610922
Gene: ABCG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88117969A= , CM000666.2:g.88117969A= GRCh38
NC_000004.11:g.89039121A= , CM000666.1:g.89039121A= GRCh37
NC_000004.10:g.89258145A= NCBI36
NG_032067.2:g.118354T=

Transcript Alleles

HGVS Amino-acid change
ENST00000237612.8:c.841+140T= MANE Select ENSP00000237612.3:n.841+140T=
ENST00000650821.1:c.841+140T= ENSP00000498246.1:n.841+140T=
ENST00000237612.7:c.841+140T= ENSP00000237612.3:n.841+140T=
ENST00000515655.5:c.841+140T= ENSP00000426917.1:n.841+140T=
NM_001257386.1:c.841+140T= NP_001244315.1:n.841+140T=
NM_004827.2:c.841+140T= NP_004818.2:n.841+140T=
XM_005263354.2:c.841+140T= XP_005263411.1:n.841+140T=
XM_005263355.2:c.841+140T= XP_005263412.1:n.841+140T=
XM_005263356.2:c.841+140T= XP_005263413.1:n.841+140T=
XM_011532420.1:c.841+140T= XP_011530722.1:n.841+140T=
NM_001257386.2:c.841+140T= NP_001244315.1:n.841+140T=
NM_001348985.1:c.841+140T= NP_001335914.1:n.841+140T=
NM_001348986.1:c.841+140T= NP_001335915.1:n.841+140T=
NM_001348987.1:c.841+140T= NP_001335916.1:n.841+140T=
NM_001348988.1:c.841+140T= NP_001335917.1:n.841+140T=
NM_001348989.1:c.841+140T= NP_001335918.1:n.841+140T=
XM_005263355.4:c.841+140T= XP_005263412.1:n.841+140T=
XM_011532420.3:c.841+140T= XP_011530722.1:n.841+140T=
XM_017008852.2:c.841+140T= XP_016864341.1:n.841+140T=
NM_004827.3:c.841+140T= MANE Select NP_004818.2:n.841+140T=
NM_001348989.2:c.841+140T= NP_001335918.1:n.841+140T=