Canonical Allele Identifier: CA2655449167
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs2147874893

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20887989A>G , CM000684.2:g.20887989A>G GRCh38
NC_000022.10:g.21242277A>G , CM000684.1:g.21242277A>G GRCh37
NC_000022.9:g.19572277A>G NCBI36
NG_012152.1:g.33986A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*153A>G MANE Select ENSP00000215730.6:n.*153A>G
ENST00000215730.11:c.*153A>G ENSP00000215730.6:n.*153A>G
NM_004782.3:c.*153A>G NP_004773.1:n.*153A>G
NM_004782.4:c.*153A>G MANE Select NP_004773.1:n.*153A>G