Canonical Allele Identifier: CA352454239
Gene: SLC6A20 HGNC NCBI

Linked Data

dbSNP Id: rs1699893308
gnomAD v3: 3-45772588-A-G
gnomAD v4: 3-45772588-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.45772588A>G , CM000665.2:g.45772588A>G GRCh38
NC_000003.11:g.45814080A>G , CM000665.1:g.45814080A>G GRCh37
NC_000003.10:g.45789084A>G NCBI36
NG_023204.1:g.28956T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703343.1:c.610T>C ENSP00000515266.1:p.Tyr204His
ENST00000358525.9:c.610T>C MANE Select ENSP00000346298.4:p.Tyr204His
ENST00000353278.8:c.583-1130T>C ENSP00000296133.5:n.583-1130T>C
ENST00000358525.8:c.610T>C ENSP00000346298.4:p.Tyr204His
ENST00000413781.1:c.469T>C ENSP00000395506.1:p.Tyr157His
ENST00000456124.6:c.610T>C ENSP00000404310.2:p.Tyr204His
NM_020208.3:c.610T>C NP_064593.1:p.Tyr204His
NM_022405.3:c.583-1130T>C NP_071800.1:n.583-1130T>C
XM_005265236.2:c.610T>C XP_005265293.1:p.Tyr204His
XM_011533847.1:c.313T>C XP_011532149.1:p.Tyr105His
XM_011533848.1:c.610T>C XP_011532150.1:p.Tyr204His
XM_011533847.2:c.313T>C XP_011532149.1:p.Tyr105His
XM_011533848.2:c.610T>C XP_011532150.1:p.Tyr204His
NM_020208.4:c.610T>C MANE Select NP_064593.1:p.Tyr204His
NM_022405.4:c.583-1130T>C NP_071800.1:n.583-1130T>C
NM_001385683.1:c.610T>C NP_001372612.1:p.Tyr204His