Canonical Allele Identifier: CA1590739028
Gene: SLC26A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981963A= , CM000667.2:g.149981963A= GRCh38
NC_000005.9:g.149361526A= , CM000667.1:g.149361526A= GRCh37
NC_000005.8:g.149341719A= NCBI36
NG_007147.2:g.23081A= , LRG_684:g.23081A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*150A= MANE Select ENSP00000286298.4:n.*150A=
ENST00000286298.4:c.*150A= ENSP00000286298.4:n.*150A=
ENST00000503336.1:c.372+3612A= ENSP00000426053.1:n.372+3612A=
NM_000112.3:c.*150A= , LRG_684t1:c.*150A= NP_000103.2:n.*150A=
XM_017009191.2:c.*47A= XP_016864680.1:n.*47A=
NM_000112.4:c.*150A= MANE Select NP_000103.2:n.*150A=
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