Canonical Allele Identifier: CA413656354
Gene: SLC16A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.73641845T>G (hg19) chrX:g.74422010T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74422010T>G , CM000685.2:g.74422010T>G GRCh38
NC_000023.10:g.73641845T>G , CM000685.1:g.73641845T>G GRCh37
NC_000023.9:g.73558570T>G NCBI36
NG_011641.1:g.5761T>G
NG_011641.2:g.5761T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.373T>G MANE Select ENSP00000465734.1:p.Tyr125Asp
ENST00000636771.1:c.119T>G
ENST00000587091.5:c.373T>G ENSP00000465734.1:p.Tyr125Asp
NM_006517.4:c.373T>G NP_006508.2:p.Tyr125Asp
XM_005262294.1:c.373T>G XP_005262351.1:p.Tyr125Asp
XM_011531015.1:c.373T>G XP_011529317.1:p.Tyr125Asp
NM_006517.5:c.373T>G MANE Select NP_006508.2:p.Tyr125Asp
Search 100 bp 5'
Search 100 bp 3'