Canonical Allele Identifier: CA2351548

Gene: SLC6A20

Linked Data

• dbSNP Id: rs766016305
• ExAC: 3:45814065 T / C
• gnomAD v2: 3-45814065-T-C
• gnomAD v3: 3-45772573-T-C
• gnomAD v4: 3-45772573-T-C
• MyVariant Identifiers: chr3:g.45814065T>C (hg19) ; chr3:g.45772573T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45772573T>C , CM000665.2:g.45772573T>C	GRCh38
NC_000003.11:g.45814065T>C , CM000665.1:g.45814065T>C	GRCh37
NC_000003.10:g.45789069T>C	NCBI36
NG_023204.1:g.28971A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703343.1:c.625A>G	ENSP00000515266.1:p.Ile209Val
ENST00000358525.9:c.625A>G MANE Select	ENSP00000346298.4:p.Ile209Val
ENST00000353278.8:c.583-1115A>G	ENSP00000296133.5:n.583-1115A>G
ENST00000358525.8:c.625A>G	ENSP00000346298.4:p.Ile209Val
ENST00000413781.1:c.484A>G	ENSP00000395506.1:p.Ile162Val
ENST00000456124.6:c.625A>G	ENSP00000404310.2:p.Ile209Val
NM_020208.3:c.625A>G	NP_064593.1:p.Ile209Val
NM_022405.3:c.583-1115A>G	NP_071800.1:n.583-1115A>G
XM_005265236.2:c.625A>G	XP_005265293.1:p.Ile209Val
XM_011533847.1:c.328A>G	XP_011532149.1:p.Ile110Val
XM_011533848.1:c.625A>G	XP_011532150.1:p.Ile209Val
XM_011533847.2:c.328A>G	XP_011532149.1:p.Ile110Val
XM_011533848.2:c.625A>G	XP_011532150.1:p.Ile209Val
NM_020208.4:c.625A>G MANE Select	NP_064593.1:p.Ile209Val
NM_022405.4:c.583-1115A>G	NP_071800.1:n.583-1115A>G
NM_001385683.1:c.625A>G	NP_001372612.1:p.Ile209Val