Canonical Allele Identifier: CA2694115312
Gene: SLC16A2 HGNC NCBI

Linked Data

gnomAD v4: X-74529165-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74529165G>T , CM000685.2:g.74529165G>T GRCh38
NC_000023.10:g.73749000G>T , CM000685.1:g.73749000G>T GRCh37
NC_000023.9:g.73665725G>T NCBI36
NG_011641.1:g.112916G>T
NG_011641.2:g.112916G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.1171-48G>T MANE Select ENSP00000465734.1:n.1171-48G>T
ENST00000636771.1:c.1080-48G>T
ENST00000587091.5:c.1171-48G>T ENSP00000465734.1:n.1171-48G>T
ENST00000590447.1:c.611-2168G>T
NM_006517.4:c.1171-48G>T NP_006508.2:n.1171-48G>T
XM_005262294.1:c.1171-2168G>T XP_005262351.1:n.1171-2168G>T
NM_006517.5:c.1171-48G>T MANE Select NP_006508.2:n.1171-48G>T