Canonical Allele Identifier: CA13014014
Gene: SLC28A3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10123041

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.84307121C>T , CM000671.2:g.84307121C>T GRCh38
NC_000009.11:g.86922036C>T , CM000671.1:g.86922036C>T GRCh37
NC_000009.10:g.86111856C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001199633.1:c.243-1776G>A VV NP_001186562.1:p.=
NM_022127.2:c.243-1776G>A VV NP_071410.1:p.=
NR_037638.2:n.565-1776G>A
XM_011518905.1:c.418+2508G>A XP_011517207.1:p.=
XM_011518906.1:c.418+2508G>A XP_011517208.1:p.=
XM_011518907.1:c.85+2508G>A XP_011517209.1:p.=
XM_011518909.1:c.418+2508G>A XP_011517211.1:p.=
XM_011518910.1:c.418+2508G>A XP_011517212.1:p.=
XR_929832.1:n.545+2508G>A
XM_011518905.2:c.418+2508G>A
XM_011518906.2:c.418+2508G>A
XM_011518907.2:c.85+2508G>A
XM_011518909.2:c.418+2508G>A
XM_011518910.2:c.418+2508G>A
XR_929832.2:n.550+2508G>A
ENST00000376238.4:c.243-1776G>A ENSP00000365413.4:p.=
ENST00000495823.1:n.445-1776G>A