Canonical Allele Identifier: CA657732862
Gene: SLC16A2 HGNC NCBI

Linked Data

gnomAD v4: X-74529180-G-A
COSMIC: COSN24861668
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74529180G>A , CM000685.2:g.74529180G>A GRCh38
NC_000023.10:g.73749015G>A , CM000685.1:g.73749015G>A GRCh37
NC_000023.9:g.73665740G>A NCBI36
NG_011641.1:g.112931G>A
NG_011641.2:g.112931G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.1171-33G>A MANE Select ENSP00000465734.1:n.1171-33G>A
ENST00000636771.1:c.1080-33G>A
ENST00000587091.5:c.1171-33G>A ENSP00000465734.1:n.1171-33G>A
ENST00000590447.1:c.611-2153G>A
NM_006517.4:c.1171-33G>A NP_006508.2:n.1171-33G>A
XM_005262294.1:c.1171-2153G>A XP_005262351.1:n.1171-2153G>A
NM_006517.5:c.1171-33G>A MANE Select NP_006508.2:n.1171-33G>A
Search 100 bp 5'
Search 100 bp 3'