Canonical Allele Identifier: CA3004471
Gene: ABCG2 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88094705C>T , CM000666.2:g.88094705C>T GRCh38
NC_000004.11:g.89015857C>T , CM000666.1:g.89015857C>T GRCh37
NC_000004.10:g.89234881C>T NCBI36
NG_032067.2:g.141618G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237612.8:c.1738-46G>A MANE Select ENSP00000237612.3:n.1738-46G>A
ENST00000650821.1:c.1738-46G>A ENSP00000498246.1:n.1738-46G>A
ENST00000237612.7:c.1738-46G>A ENSP00000237612.3:n.1738-46G>A
ENST00000515655.5:c.1728-46G>A ENSP00000426917.1:n.1728-46G>A
NM_001257386.1:c.1728-46G>A NP_001244315.1:n.1728-46G>A
NM_004827.2:c.1738-46G>A NP_004818.2:n.1738-46G>A
XM_005263354.2:c.1738-46G>A XP_005263411.1:n.1738-46G>A
XM_005263355.2:c.1738-46G>A XP_005263412.1:n.1738-46G>A
XM_005263356.2:c.1732-46G>A XP_005263413.1:n.1732-46G>A
XM_011532420.1:c.1738-46G>A XP_011530722.1:n.1738-46G>A
NM_001257386.2:c.1728-46G>A NP_001244315.1:n.1728-46G>A
NM_001348985.1:c.1738-46G>A NP_001335914.1:n.1738-46G>A
NM_001348986.1:c.1738-46G>A NP_001335915.1:n.1738-46G>A
NM_001348987.1:c.1732-46G>A NP_001335916.1:n.1732-46G>A
NM_001348988.1:c.1738-46G>A NP_001335917.1:n.1738-46G>A
NM_001348989.1:c.1738-46G>A NP_001335918.1:n.1738-46G>A
XM_005263355.4:c.1738-46G>A XP_005263412.1:n.1738-46G>A
XM_011532420.3:c.1738-46G>A XP_011530722.1:n.1738-46G>A
XM_017008852.2:c.1732-46G>A XP_016864341.1:n.1732-46G>A
NM_004827.3:c.1738-46G>A MANE Select NP_004818.2:n.1738-46G>A
NM_001348989.2:c.1738-46G>A NP_001335918.1:n.1738-46G>A