Canonical Allele Identifier: CA413658489
Gene: SLC16A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.73749201A>C (hg19) chrX:g.74529366A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74529366A>C , CM000685.2:g.74529366A>C GRCh38
NC_000023.10:g.73749201A>C , CM000685.1:g.73749201A>C GRCh37
NC_000023.9:g.73665926A>C NCBI36
NG_011641.1:g.113117A>C
NG_011641.2:g.113117A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1324A>C MANE Select ENSP00000465734.1:p.Met442Leu
ENST00000636771.1:c.1233A>C
ENST00000587091.5:c.1324A>C ENSP00000465734.1:p.Met442Leu
ENST00000590447.1:c.611-1967A>C
NM_006517.4:c.1324A>C NP_006508.2:p.Met442Leu
XM_005262294.1:c.1171-1967A>C XP_005262351.1:n.1171-1967A>C
NM_006517.5:c.1324A>C MANE Select NP_006508.2:p.Met442Leu
Search 100 bp 5'
Search 100 bp 3'