Canonical Allele Identifier: CA433447630

Gene: SLC6A20

Linked Data

• MyVariant Identifiers: chr3:g.45814021G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45772529G>C , CM000665.2:g.45772529G>C	GRCh38
NC_000003.11:g.45814021G>C , CM000665.1:g.45814021G>C	GRCh37
NC_000003.10:g.45789025G>C	NCBI36
NG_023204.1:g.29015C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703343.1:c.669C>G	ENSP00000515266.1:p.Gly223=
ENST00000358525.9:c.669C>G MANE Select	ENSP00000346298.4:p.Gly223=
ENST00000353278.8:c.583-1071C>G	ENSP00000296133.5:n.583-1071C>G
ENST00000358525.8:c.669C>G	ENSP00000346298.4:p.Gly223=
ENST00000413781.1:c.528C>G	ENSP00000395506.1:p.Gly176=
ENST00000456124.6:c.669C>G	ENSP00000404310.2:p.Gly223=
NM_020208.3:c.669C>G	NP_064593.1:p.Gly223=
NM_022405.3:c.583-1071C>G	NP_071800.1:n.583-1071C>G
XM_005265236.2:c.669C>G	XP_005265293.1:p.Gly223=
XM_011533847.1:c.372C>G	XP_011532149.1:p.Gly124=
XM_011533848.1:c.669C>G	XP_011532150.1:p.Gly223=
XM_011533847.2:c.372C>G	XP_011532149.1:p.Gly124=
XM_011533848.2:c.669C>G	XP_011532150.1:p.Gly223=
NM_020208.4:c.669C>G MANE Select	NP_064593.1:p.Gly223=
NM_022405.4:c.583-1071C>G	NP_071800.1:n.583-1071C>G
NM_001385683.1:c.669C>G	NP_001372612.1:p.Gly223=