Canonical Allele Identifier: CA340270
Gene: HPS3 HGNC NCBI

Linked Data

ClinVar Variation Id: 4610
ClinVar RCV Id: RCV000004873
dbSNP Id: rs281865093

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149157533T>G , CM000665.2:g.149157533T>G GRCh38
NC_000003.11:g.148875320T>G , CM000665.1:g.148875320T>G GRCh37
NC_000003.10:g.150358010T>G NCBI36
NG_009847.1:g.32950T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296051.7:c.1691+2T>G MANE Select ENSP00000296051.2:n.1691+2T>G
ENST00000296051.6:c.1691+2T>G ENSP00000296051.2:n.1691+2T>G
ENST00000460120.5:c.1196+2T>G ENSP00000418230.1:n.1196+2T>G
NM_001308258.1:c.1196+2T>G NP_001295187.1:n.1196+2T>G
NM_032383.3:c.1691+2T>G NP_115759.2:n.1691+2T>G
NM_032383.4:c.1691+2T>G NP_115759.2:n.1691+2T>G
XM_005247834.3:c.1691+2T>G XP_005247891.1:n.1691+2T>G
XM_006713788.1:c.1691+2T>G XP_006713851.1:n.1691+2T>G
XR_924201.1:n.1806+2T>G
XM_005247834.4:c.1691+2T>G XP_005247891.1:n.1691+2T>G
XM_017007323.2:c.1691+2T>G XP_016862812.1:n.1691+2T>G
XR_001740326.2:n.1791+2T>G
XR_001740327.2:n.1791+2T>G
XR_001740328.2:n.1791+2T>G
XR_924201.3:n.1791+2T>G
NM_001308258.2:c.1196+2T>G NP_001295187.1:n.1196+2T>G
NM_032383.5:c.1691+2T>G MANE Select NP_115759.2:n.1691+2T>G