Canonical Allele Identifier: CA2396589460
Gene: SNAP29 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888078G= , CM000684.2:g.20888078G= GRCh38
NC_000022.10:g.21242366G= , CM000684.1:g.21242366G= GRCh37
NC_000022.9:g.19572366G= NCBI36
NG_012152.1:g.34075G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*242G= MANE Select ENSP00000215730.6:n.*242G=
ENST00000215730.11:c.*242G= ENSP00000215730.6:n.*242G=
NM_004782.3:c.*242G= NP_004773.1:n.*242G=
NM_004782.4:c.*242G= MANE Select NP_004773.1:n.*242G=
Search 100 bp 5'
Search 100 bp 3'