Canonical Allele Identifier: CA3357933
Gene: SLCO6A1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10073892

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.102391066T>C , CM000667.2:g.102391066T>C GRCh38
NC_000005.9:g.101726770T>C , CM000667.1:g.101726770T>C GRCh37
NC_000005.8:g.101754669T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001289002.1:c.1815-21A>G VV NP_001275931.1:p.=
NM_001289004.1:c.1629-21A>G VV NP_001275933.1:p.=
NM_001308014.1:c.1056-21A>G VV NP_001294943.1:p.=
NM_173488.4:c.1815-21A>G VV NP_775759.3:p.=
XM_005271874.2:c.1815-21A>G XP_005271931.1:p.=
XM_011543147.1:c.1710-21A>G XP_011541449.1:p.=
XM_011543148.1:c.1578-21A>G XP_011541450.1:p.=
XM_011543149.1:c.1242-21A>G XP_011541451.1:p.=
XM_011543150.1:c.1086-21A>G XP_011541452.1:p.=
XM_011543151.1:c.1056-21A>G XP_011541453.1:p.=
XM_011543153.1:c.993-21A>G XP_011541455.1:p.=
XM_005271874.3:c.1815-21A>G
XM_011543147.2:c.1710-21A>G
XM_011543148.2:c.1578-21A>G
XM_011543153.2:c.993-21A>G
ENST00000379807.7:c.1815-21A>G ENSP00000369135.3:p.=
ENST00000389019.7:c.1629-21A>G ENSP00000373671.3:p.=
ENST00000506729.5:c.1815-21A>G ENSP00000421339.1:p.=
ENST00000513675.1:c.1056-21A>G ENSP00000421990.1:p.=
ENST00000514765.6:n.164A>G