Canonical Allele Identifier: CA10612768

Gene: SCN9A SCN1A-AS1

Linked Data

• ClinVar Variation Id: 331918
• ClinVar RCV Id: RCV000342600 ; RCV000357374 ; RCV000394741 ; RCV000398622
• dbSNP Id: rs201184093
• gnomAD v2: 2-167052991-C-T
• gnomAD v3: 2-166196481-C-T
• gnomAD v4: 2-166196481-C-T
• MyVariant Identifiers: chr2:g.167052991C>T (hg19) ; chr2:g.166196481C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.166196481C>T , CM000664.2:g.166196481C>T	GRCh38
NC_000002.11:g.167052991C>T , CM000664.1:g.167052991C>T	GRCh37
NC_000002.10:g.166761237C>T	NCBI36
NG_012798.1:g.184507G>A , LRG_369:g.184507G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303354.11:c.*2191G>A (SCN9A)	ENSP00000304748.7:n.*2191G>A
ENST00000642356.2:c.*2191G>A (SCN9A) MANE Select	ENSP00000495601.1:n.*2191G>A
ENST00000303354.10:c.*2191G>A (SCN9A)	ENSP00000304748.7:n.*2191G>A
ENST00000409672.5:c.*2191G>A (SCN9A)	ENSP00000386306.1:n.*2191G>A
NM_002977.3:c.*2191G>A , LRG_369t1:c.*2191G>A (SCN9A)	NP_002968.1:n.*2191G>A
NR_110260.1:n.432-3158C>T (SCN1A-AS1)
NM_001365536.1:c.*2191G>A (SCN9A) MANE Select	NP_001352465.1:n.*2191G>A