Canonical Allele Identifier: CA1126194568
Gene: SLC28A3 HGNC NCBI

Linked Data

dbSNP Id: rs1825349425
gnomAD v3: 9-84294622-T-C
gnomAD v4: 9-84294622-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.84294622T>C , CM000671.2:g.84294622T>C GRCh38
NC_000009.11:g.86909537T>C , CM000671.1:g.86909537T>C GRCh37
NC_000009.10:g.86099357T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376238.5:c.862-347A>G MANE Select ENSP00000365413.4:n.862-347A>G
ENST00000376238.4:c.862-347A>G ENSP00000365413.4:n.862-347A>G
NM_001199633.1:c.862-347A>G NP_001186562.1:n.862-347A>G
NM_022127.2:c.862-347A>G NP_071410.1:n.862-347A>G
NR_037638.2:n.1184-347A>G
XM_011518905.1:c.946-347A>G XP_011517207.1:n.946-347A>G
XM_011518906.1:c.946-347A>G XP_011517208.1:n.946-347A>G
XM_011518907.1:c.613-347A>G XP_011517209.1:n.613-347A>G
XM_011518908.1:c.223-347A>G XP_011517210.1:n.223-347A>G
XM_011518909.1:c.946-347A>G XP_011517211.1:n.946-347A>G
XM_011518910.1:c.946-347A>G XP_011517212.1:n.946-347A>G
XR_929832.1:n.1073-347A>G
XM_011518905.2:c.946-347A>G XP_011517207.1:n.946-347A>G
XM_011518906.2:c.946-347A>G XP_011517208.1:n.946-347A>G
XM_011518907.2:c.613-347A>G XP_011517209.1:n.613-347A>G
XM_011518908.2:c.223-347A>G XP_011517210.1:n.223-347A>G
XM_011518909.2:c.946-347A>G XP_011517211.1:n.946-347A>G
XM_011518910.2:c.946-347A>G XP_011517212.1:n.946-347A>G
XR_929832.2:n.1078-347A>G
NM_001199633.2:c.862-347A>G MANE Select NP_001186562.1:n.862-347A>G
NM_022127.3:c.862-347A>G NP_071410.1:n.862-347A>G
NR_037638.3:n.1163-347A>G