Canonical Allele Identifier: CA2694115310
Gene: SLC16A2 HGNC NCBI

Linked Data

gnomAD v4: X-74529162-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74529162T>A , CM000685.2:g.74529162T>A GRCh38
NC_000023.10:g.73748997T>A , CM000685.1:g.73748997T>A GRCh37
NC_000023.9:g.73665722T>A NCBI36
NG_011641.1:g.112913T>A
NG_011641.2:g.112913T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1171-51T>A MANE Select ENSP00000465734.1:n.1171-51T>A
ENST00000636771.1:c.1080-51T>A
ENST00000587091.5:c.1171-51T>A ENSP00000465734.1:n.1171-51T>A
ENST00000590447.1:c.611-2171T>A
NM_006517.4:c.1171-51T>A NP_006508.2:n.1171-51T>A
XM_005262294.1:c.1171-2171T>A XP_005262351.1:n.1171-2171T>A
NM_006517.5:c.1171-51T>A MANE Select NP_006508.2:n.1171-51T>A
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