Canonical Allele Identifier: CA1000197400
Gene: SERINC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.31411078T>A , CM000663.2:g.31411078T>A GRCh38
NC_000001.10:g.31883925T>A , CM000663.1:g.31883925T>A GRCh37
NC_000001.9:g.31656512T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000373710.5:c.66+643T>A ENSP00000362814.1:n.66+643T>A
ENST00000487207.5:n.219+643T>A
ENST00000536859.5:c.51+643T>A ENSP00000444307.1:n.51+643T>A
NM_001199037.1:c.51+643T>A NP_001185966.1:n.51+643T>A
NM_001199038.1:c.66+643T>A NP_001185967.1:n.66+643T>A
NM_001199038.2:c.66+643T>A NP_001185967.1:n.66+643T>A
NM_001199037.2:c.51+643T>A NP_001185966.1:n.51+643T>A