Canonical Allele Identifier: CA2527307578
Gene: SNAPIN HGNC NCBI

Linked Data

dbSNP Id: rs2101708990

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153660658A>G , CM000663.2:g.153660658A>G GRCh38
NC_000001.10:g.153633134A>G , CM000663.1:g.153633134A>G GRCh37
NC_000001.9:g.151899758A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368685.6:c.310-542A>G MANE Select ENSP00000357674.5:n.310-542A>G
ENST00000368685.5:c.310-542A>G ENSP00000357674.5:n.310-542A>G
ENST00000462880.1:n.293-542A>G
ENST00000474959.5:n.593-542A>G
ENST00000478558.1:n.841-542A>G
NM_012437.5:c.310-542A>G NP_036569.1:n.310-542A>G
NR_052019.1:n.353-542A>G
NR_052020.1:n.339-542A>G
NM_012437.6:c.310-542A>G MANE Select NP_036569.1:n.310-542A>G