Canonical Allele Identifier: CA2694115168
Gene: SLC16A2 HGNC NCBI

Linked Data

gnomAD v4: X-74525688-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525688G>T , CM000685.2:g.74525688G>T GRCh38
NC_000023.10:g.73745523G>T , CM000685.1:g.73745523G>T GRCh37
NC_000023.9:g.73662248G>T NCBI36
NG_011641.1:g.109439G>T
NG_011641.2:g.109439G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1027-62G>T MANE Select ENSP00000465734.1:n.1027-62G>T
ENST00000636771.1:c.936-62G>T
ENST00000587091.5:c.1027-62G>T ENSP00000465734.1:n.1027-62G>T
ENST00000590447.1:c.467-62G>T
NM_006517.4:c.1027-62G>T NP_006508.2:n.1027-62G>T
XM_005262294.1:c.1027-62G>T XP_005262351.1:n.1027-62G>T
XM_011531015.1:c.*31-62G>T XP_011529317.1:n.*31-62G>T
NM_006517.5:c.1027-62G>T MANE Select NP_006508.2:n.1027-62G>T
Search 100 bp 5'
Search 100 bp 3'