Canonical Allele Identifier: CA382769050
Gene: SCN2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118039385G>C (hg19) chr11:g.118168670G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118168670G>C , CM000673.2:g.118168670G>C GRCh38
NC_000011.9:g.118039385G>C , CM000673.1:g.118039385G>C GRCh37
NC_000011.8:g.117544595G>C NCBI36
NG_042217.1:g.12953C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000278947.6:c.152C>G MANE Select ENSP00000278947.5:p.Thr51Ser
ENST00000658882.1:c.256C>G ENSP00000499572.1:p.Pro86Ala
ENST00000665446.1:n.388C>G
ENST00000669850.1:n.394C>G
ENST00000278947.5:c.152C>G ENSP00000278947.5:p.Thr51Ser
NM_004588.4:c.152C>G NP_004579.1:p.Thr51Ser
NM_004588.5:c.152C>G MANE Select NP_004579.1:p.Thr51Ser
Search 100 bp 5'
Search 100 bp 3'