Canonical Allele Identifier: CA896320696
Gene: SEC13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10294607G>C , CM000665.2:g.10294607G>C GRCh38
NC_000003.11:g.10336291G>C , CM000665.1:g.10336291G>C GRCh37
NC_000003.10:g.10311291G>C NCBI36
NG_011560.1:g.3341C>G
NG_033090.1:g.18656G>C
NG_033090.2:g.18656G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000492602.5:n.188-1271C>G