Canonical Allele Identifier: CA403460786

Gene: SEMA6B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4543953C>G , CM000681.2:g.4543953C>G	GRCh38
NC_000019.9:g.4543965C>G , CM000681.1:g.4543965C>G	GRCh37
NC_000019.8:g.4494965C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032108.4:c.2315G>C MANE Select	NP_115484.2:p.Gly772Ala
ENST00000586582.6:c.2315G>C MANE Select	ENSP00000467290.1:p.Gly772Ala
NM_032108.3:c.2315G>C	NP_115484.2:p.Gly772Ala
ENST00000586582.5:c.2315G>C	ENSP00000467290.1:p.Gly772Ala
ENST00000586965.1:c.1851+464G>C	ENSP00000465722.1:n.1851+464G>C
ENST00000676793.1:c.2315G>C	ENSP00000503414.1:p.Gly772Ala
ENST00000677828.1:c.*1577G>C	ENSP00000503277.1:n.*1577G>C
XM_011527639.1:c.2333G>C	XP_011525941.1:p.Gly778Ala
XM_011527639.2:c.2333G>C	XP_011525941.1:p.Gly778Ala
XM_011527640.1:c.2333G>C	XP_011525942.1:p.Gly778Ala
XM_011527640.2:c.2333G>C	XP_011525942.1:p.Gly778Ala