Canonical Allele Identifier: CA2579647155
Gene: SLC16A2 HGNC NCBI

Linked Data

gnomAD v4: X-74525663-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525663G>A , CM000685.2:g.74525663G>A GRCh38
NC_000023.10:g.73745498G>A , CM000685.1:g.73745498G>A GRCh37
NC_000023.9:g.73662223G>A NCBI36
NG_011641.1:g.109414G>A
NG_011641.2:g.109414G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1027-87G>A MANE Select ENSP00000465734.1:n.1027-87G>A
ENST00000636771.1:c.936-87G>A
ENST00000587091.5:c.1027-87G>A ENSP00000465734.1:n.1027-87G>A
ENST00000590447.1:c.467-87G>A
NM_006517.4:c.1027-87G>A NP_006508.2:n.1027-87G>A
XM_005262294.1:c.1027-87G>A XP_005262351.1:n.1027-87G>A
XM_011531015.1:c.*31-87G>A XP_011529317.1:n.*31-87G>A
NM_006517.5:c.1027-87G>A MANE Select NP_006508.2:n.1027-87G>A
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