Canonical Allele Identifier: CA354618034
Community Standard Title: NM_005630.3(SLCO2A1):c.621C>A (p.Tyr207Ter)
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133954970G>T , CM000665.2:g.133954970G>T GRCh38
NC_000003.11:g.133673814G>T , CM000665.1:g.133673814G>T GRCh37
NC_000003.10:g.135156504G>T NCBI36
NG_031964.2:g.102215C>A
NG_031964.3:g.102215C>A

Transcript Alleles

HGVS Amino-acid Change
NM_005630.3:c.621C>A MANE Select NP_005621.2:p.Tyr207Ter
ENST00000310926.11:c.621C>A MANE Select ENSP00000311291.4:p.Tyr207Ter
NM_005630.2:c.621C>A NP_005621.2:p.Tyr207Ter
ENST00000310926.8:c.621C>A ENSP00000311291.4:p.Tyr207Ter
ENST00000462770.5:n.521-6270C>A
ENST00000464676.5:n.883C>A
ENST00000481359.3:c.621C>A ENSP00000420028.3:p.Tyr207Ter
ENST00000493729.5:c.398-1209C>A ENSP00000418893.1:n.398-1209C>A
XM_011513090.1:c.621C>A XP_011511392.1:p.Tyr207Ter
XM_017007077.1:c.117C>A XP_016862566.1:p.Tyr39Ter
XM_024453721.1:c.621C>A XP_024309489.1:p.Tyr207Ter