Canonical Allele Identifier: CA361708885
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1412248637

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981403G>T , CM000667.2:g.149981403G>T GRCh38
NC_000005.9:g.149360966G>T , CM000667.1:g.149360966G>T GRCh37
NC_000005.8:g.149341159G>T NCBI36
NG_007147.2:g.22521G>T , LRG_684:g.22521G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.1810G>T MANE Select ENSP00000286298.4:p.Val604Phe
ENST00000286298.4:c.1810G>T ENSP00000286298.4:p.Val604Phe
ENST00000503336.1:c.372+3052G>T ENSP00000426053.1:n.372+3052G>T
NM_000112.3:c.1810G>T , LRG_684t1:c.1810G>T NP_000103.2:p.Val604Phe
XM_017009191.2:c.1810G>T XP_016864680.1:p.Val604Phe
NM_000112.4:c.1810G>T MANE Select NP_000103.2:p.Val604Phe