Canonical Allele Identifier: CA799613424

Gene: ABCG2

Linked Data

• dbSNP Id: rs557281274
• MyVariant Identifiers: chr4:g.89052127G>A (hg19) ; chr4:g.88130975G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88130975G>A , CM000666.2:g.88130975G>A	GRCh38
NC_000004.11:g.89052127G>A , CM000666.1:g.89052127G>A	GRCh37
NC_000004.10:g.89271151G>A	NCBI36
NG_032067.2:g.105348C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237612.8:c.531+86C>T MANE Select	ENSP00000237612.3:n.531+86C>T
ENST00000650821.1:c.531+86C>T	ENSP00000498246.1:n.531+86C>T
ENST00000237612.7:c.531+86C>T	ENSP00000237612.3:n.531+86C>T
ENST00000515655.5:c.531+86C>T	ENSP00000426917.1:n.531+86C>T
NM_001257386.1:c.531+86C>T	NP_001244315.1:n.531+86C>T
NM_004827.2:c.531+86C>T	NP_004818.2:n.531+86C>T
XM_005263354.2:c.531+86C>T	XP_005263411.1:n.531+86C>T
XM_005263355.2:c.531+86C>T	XP_005263412.1:n.531+86C>T
XM_005263356.2:c.531+86C>T	XP_005263413.1:n.531+86C>T
XM_011532420.1:c.531+86C>T	XP_011530722.1:n.531+86C>T
NM_001257386.2:c.531+86C>T	NP_001244315.1:n.531+86C>T
NM_001348985.1:c.531+86C>T	NP_001335914.1:n.531+86C>T
NM_001348986.1:c.531+86C>T	NP_001335915.1:n.531+86C>T
NM_001348987.1:c.531+86C>T	NP_001335916.1:n.531+86C>T
NM_001348988.1:c.531+86C>T	NP_001335917.1:n.531+86C>T
NM_001348989.1:c.531+86C>T	NP_001335918.1:n.531+86C>T
XM_005263355.4:c.531+86C>T	XP_005263412.1:n.531+86C>T
XM_011532420.3:c.531+86C>T	XP_011530722.1:n.531+86C>T
XM_017008852.2:c.531+86C>T	XP_016864341.1:n.531+86C>T
NM_004827.3:c.531+86C>T MANE Select	NP_004818.2:n.531+86C>T
NM_001348989.2:c.531+86C>T	NP_001335918.1:n.531+86C>T