Canonical Allele Identifier: CA361704990
Gene: SLC26A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.149357652T>C (hg19) chr5:g.149978089T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978089T>C , CM000667.2:g.149978089T>C GRCh38
NC_000005.9:g.149357652T>C , CM000667.1:g.149357652T>C GRCh37
NC_000005.8:g.149337845T>C NCBI36
NG_007147.2:g.19207T>C , LRG_684:g.19207T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.669T>C
ENST00000286298.5:c.437T>C MANE Select ENSP00000286298.4:p.Phe146Ser
ENST00000286298.4:c.437T>C ENSP00000286298.4:p.Phe146Ser
ENST00000503336.1:c.110T>C ENSP00000426053.1:p.Phe37Ser
NM_000112.3:c.437T>C , LRG_684t1:c.437T>C NP_000103.2:p.Phe146Ser
XM_017009191.2:c.437T>C XP_016864680.1:p.Phe146Ser
NM_000112.4:c.437T>C MANE Select NP_000103.2:p.Phe146Ser
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