Canonical Allele Identifier: CA2706194959
Gene: ABCG2 HGNC NCBI

Linked Data

dbSNP Id: rs1429431387
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169593G>A , CM000666.2:g.88169593G>A GRCh38
NC_000004.11:g.89090745G>A , CM000666.1:g.89090745G>A GRCh37
NC_000004.10:g.89309769G>A NCBI36
NG_032067.2:g.66730C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650821.1:c.-19-29579C>T ENSP00000498246.1:n.-19-29579C>T
ENST00000515655.5:c.-19-29579C>T ENSP00000426917.1:n.-19-29579C>T
NM_001257386.1:c.-19-29579C>T NP_001244315.1:n.-19-29579C>T
XM_005263355.2:c.-19-29579C>T XP_005263412.1:n.-19-29579C>T
XM_011532420.1:c.-19-29579C>T XP_011530722.1:n.-19-29579C>T
NM_001257386.2:c.-19-29579C>T NP_001244315.1:n.-19-29579C>T
NM_001348985.1:c.-19-29579C>T NP_001335914.1:n.-19-29579C>T
XM_005263355.4:c.-19-29579C>T XP_005263412.1:n.-19-29579C>T
XM_011532420.3:c.-19-29579C>T XP_011530722.1:n.-19-29579C>T
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