Canonical Allele Identifier: CA322277838
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1037226907
gnomAD v2: 22-21242808-C-G
gnomAD v3: 22-20888520-C-G
gnomAD v4: 22-20888520-C-G
MyVariant Identifiers: chr22:g.21242808C>G (hg19) chr22:g.20888520C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888520C>G , CM000684.2:g.20888520C>G GRCh38
NC_000022.10:g.21242808C>G , CM000684.1:g.21242808C>G GRCh37
NC_000022.9:g.19572808C>G NCBI36
NG_012152.1:g.34517C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*684C>G MANE Select ENSP00000215730.6:n.*684C>G
ENST00000215730.11:c.*684C>G ENSP00000215730.6:n.*684C>G
NM_004782.3:c.*684C>G NP_004773.1:n.*684C>G
NM_004782.4:c.*684C>G MANE Select NP_004773.1:n.*684C>G
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