Canonical Allele Identifier: CA509826672
Gene: SEC23B HGNC NCBI

Linked Data

dbSNP Id: rs2148899953
MyVariant Identifiers: chr20:g.18507052G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.18526408G>C , CM000682.2:g.18526408G>C GRCh38
NC_000020.10:g.18507052G>C , CM000682.1:g.18507052G>C GRCh37
NC_000020.9:g.18455052G>C NCBI36
NG_016281.1:g.23865G>C
NG_016281.2:g.23927G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000336714.8:c.870G>C ENSP00000338844.3:p.Leu290=
ENST00000377465.6:c.870G>C ENSP00000366685.1:p.Leu290=
ENST00000450074.6:c.870G>C ENSP00000403971.1:p.Leu290=
ENST00000643747.1:c.816G>C ENSP00000496460.1:p.Leu272=
ENST00000650089.1:c.870G>C MANE Select ENSP00000497473.1:p.Leu290=
ENST00000262544.6:c.870G>C ENSP00000262544.2:p.Leu290=
ENST00000336714.7:c.870G>C ENSP00000338844.3:p.Leu290=
ENST00000377465.5:c.870G>C ENSP00000366685.1:p.Leu290=
ENST00000377475.7:c.870G>C ENSP00000366695.3:p.Leu290=
ENST00000450074.5:c.870G>C ENSP00000403971.1:p.Leu290=
NM_001172745.1:c.870G>C NP_001166216.1:p.Leu290=
NM_001172746.1:c.816G>C NP_001166217.1:p.Leu272=
NM_006363.4:c.870G>C NP_006354.2:p.Leu290=
NM_032985.4:c.870G>C NP_116780.1:p.Leu290=
NM_032986.3:c.870G>C NP_116781.1:p.Leu290=
NM_001172745.2:c.870G>C NP_001166216.1:p.Leu290=
NM_001172746.2:c.816G>C NP_001166217.1:p.Leu272=
NM_006363.6:c.870G>C MANE Select NP_006354.2:p.Leu290=
NM_032985.5:c.870G>C NP_116780.1:p.Leu290=
NM_032986.4:c.870G>C NP_116781.1:p.Leu290=
XM_017027593.1:c.870G>C XP_016883082.1:p.Leu290=
NM_001172745.3:c.870G>C NP_001166216.1:p.Leu290=
NM_001172746.3:c.816G>C NP_001166217.1:p.Leu272=
NM_032985.6:c.870G>C NP_116780.1:p.Leu290=
NM_032986.5:c.870G>C NP_116781.1:p.Leu290=