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Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.4762607C>T , CM000678.2:g.4762607C>T
GRCh38
NC_000016.9:g.4812608C>T , CM000678.1:g.4812608C>T
GRCh37
NC_000016.8:g.4752609C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000219478.11:c.564G>A
MANE Select
ENSP00000219478.5:p.Arg188=
ENST00000219478.10:c.564G>A
ENSP00000219478.5:p.Arg188=
ENST00000545009.1:c.564G>A
ENSP00000445714.1:p.Arg188=
ENST00000589422.1:c.*92G>A
ENSP00000466375.1:n.*92G>A
NM_001303450.1:c.564G>A
NP_001290379.1:p.Arg188=
NM_021646.2:c.564G>A
NP_067678.1:p.Arg188=
XM_005255243.2:c.213G>A
XP_005255300.1:p.Arg71=
XM_011522453.1:c.564G>A
XP_011520755.1:p.Arg188=
XM_011522454.1:c.-61G>A
XP_011520756.1:n.-61G>A
NM_021646.3:c.564G>A
NP_067678.1:p.Arg188=
XM_005255243.4:c.213G>A
XP_005255300.1:p.Arg71=
XM_011522453.2:c.564G>A
XP_011520755.1:p.Arg188=
XM_011522454.3:c.-61G>A
XP_011520756.1:n.-61G>A
XM_017023121.2:c.-61G>A
XP_016878610.1:n.-61G>A
NM_001303450.2:c.564G>A
NP_001290379.1:p.Arg188=
NM_021646.4:c.564G>A
MANE Select
NP_067678.1:p.Arg188=