Canonical Allele Identifier: CA751562935
Gene: SNAP29 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*684C>T MANE Select ENSP00000215730.6:n.*684C>T
ENST00000215730.11:c.*684C>T ENSP00000215730.6:n.*684C>T
NM_004782.3:c.*684C>T NP_004773.1:n.*684C>T
NM_004782.4:c.*684C>T MANE Select NP_004773.1:n.*684C>T
Search 100 bp 5'
Search 100 bp 3'