Canonical Allele Identifier: CA2396589394
Gene: SNAP29 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20887950G= , CM000684.2:g.20887950G= GRCh38
NC_000022.10:g.21242238G= , CM000684.1:g.21242238G= GRCh37
NC_000022.9:g.19572238G= NCBI36
NG_012152.1:g.33947G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*114G= MANE Select ENSP00000215730.6:n.*114G=
ENST00000215730.11:c.*114G= ENSP00000215730.6:n.*114G=
NM_004782.3:c.*114G= NP_004773.1:n.*114G=
NM_004782.4:c.*114G= MANE Select NP_004773.1:n.*114G=
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