Canonical Allele Identifier: CA7289134
Gene: SPTLC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 314666
ClinVar RCV Id: RCV000358260
dbSNP Id: rs577069180
ExAC: 14:77984373 C / A
gnomAD v2: 14-77984373-C-A
gnomAD v3: 14-77518030-C-A
gnomAD v4: 14-77518030-C-A
MyVariant Identifiers: chr14:g.77984373C>A (hg19) chr14:g.77518030C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77518030C>A , CM000676.2:g.77518030C>A GRCh38
NC_000014.8:g.77984373C>A , CM000676.1:g.77984373C>A GRCh37
NC_000014.7:g.77054126C>A NCBI36
NG_028282.1:g.103738G>T , LRG_371:g.103738G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000686627.1:n.601+8G>T
ENST00000687688.1:n.1332+8G>T
ENST00000692906.1:n.1301+8G>T
ENST00000216484.7:c.1569+8G>T MANE Select ENSP00000216484.2:n.1569+8G>T
ENST00000216484.6:c.1569+8G>T ENSP00000216484.2:n.1569+8G>T
ENST00000556607.1:c.397+8G>T ENSP00000451029.1:n.397+8G>T
NM_004863.3:c.1569+8G>T , LRG_371t1:c.1569+8G>T NP_004854.1:n.1569+8G>T
NM_004863.4:c.1569+8G>T MANE Select NP_004854.1:n.1569+8G>T
Search 100 bp 5'
Search 100 bp 3'