Canonical Allele Identifier: CA322277572

Gene: SNAP29

Linked Data

• dbSNP Id: rs974803237
• gnomAD v2: 22-21242559-G-C
• gnomAD v4: 22-20888271-G-C
• MyVariant Identifiers: chr22:g.21242559G>C (hg19) ; chr22:g.20888271G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888271G>C , CM000684.2:g.20888271G>C	GRCh38
NC_000022.10:g.21242559G>C , CM000684.1:g.21242559G>C	GRCh37
NC_000022.9:g.19572559G>C	NCBI36
NG_012152.1:g.34268G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*435G>C MANE Select	ENSP00000215730.6:n.*435G>C
ENST00000215730.11:c.*435G>C	ENSP00000215730.6:n.*435G>C
NM_004782.3:c.*435G>C	NP_004773.1:n.*435G>C
NM_004782.4:c.*435G>C MANE Select	NP_004773.1:n.*435G>C