Canonical Allele Identifier: CA361704377
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1217971274
gnomAD v2: 5-149357423-G-C
gnomAD v3: 5-149977860-G-C
gnomAD v4: 5-149977860-G-C
MyVariant Identifiers: chr5:g.149357423G>C (hg19) chr5:g.149977860G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977860G>C , CM000667.2:g.149977860G>C GRCh38
NC_000005.9:g.149357423G>C , CM000667.1:g.149357423G>C GRCh37
NC_000005.8:g.149337616G>C NCBI36
NG_007147.2:g.18978G>C , LRG_684:g.18978G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000690410.1:n.440G>C
ENST00000286298.5:c.208G>C MANE Select ENSP00000286298.4:p.Val70Leu
ENST00000286298.4:c.208G>C ENSP00000286298.4:p.Val70Leu
NM_000112.3:c.208G>C , LRG_684t1:c.208G>C NP_000103.2:p.Val70Leu
XM_017009191.2:c.208G>C XP_016864680.1:p.Val70Leu
NM_000112.4:c.208G>C MANE Select NP_000103.2:p.Val70Leu
Search 100 bp 5'
Search 100 bp 3'