Canonical Allele Identifier: CA3505243
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs777500286

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978074T>C , CM000667.2:g.149978074T>C GRCh38
NC_000005.9:g.149357637T>C , CM000667.1:g.149357637T>C GRCh37
NC_000005.8:g.149337830T>C NCBI36
NG_007147.2:g.19192T>C , LRG_684:g.19192T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.654T>C
ENST00000286298.5:c.422T>C MANE Select ENSP00000286298.4:p.Leu141Pro
ENST00000286298.4:c.422T>C ENSP00000286298.4:p.Leu141Pro
ENST00000503336.1:c.95T>C ENSP00000426053.1:p.Leu32Pro
NM_000112.3:c.422T>C , LRG_684t1:c.422T>C NP_000103.2:p.Leu141Pro
XM_017009191.2:c.422T>C XP_016864680.1:p.Leu141Pro
NM_000112.4:c.422T>C MANE Select NP_000103.2:p.Leu141Pro