Canonical Allele Identifier: CA6909705
Gene: SGCG HGNC NCBI
MyVariant.info:
GRCh38 chr13:g.23279493G>A
GRCh37 chr13:g.23853632G>A
gnomAD v2:
13:23853632 G / A
gnomAD v3:
13:23279493 G / A
gnomAD v4:
chr13-23279493-G-A
Joint Max Group AF 0.00165225 (AFR)
Genomes Max Group AF 0.00136733 (AFR)
Exomes Max Group AF 0.00178137 (AFR)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23279493G>A , CM000675.2:g.23279493G>A GRCh38
NC_000013.10:g.23853632G>A , CM000675.1:g.23853632G>A GRCh37
NC_000013.9:g.22751632G>A NCBI36
NG_008759.1:g.103573G>A , LRG_207:g.103573G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218867.4:c.505+15G>A MANE Select ENSP00000218867.3:n.505+15G>A
ENST00000218867.3:c.505+15G>A ENSP00000218867.3:n.505+15G>A
NM_000231.2:c.505+15G>A , LRG_207t1:c.505+15G>A NP_000222.1:n.505+15G>A
XM_005266505.2:c.505+15G>A XP_005266562.1:n.505+15G>A
XM_006719861.2:c.559+15G>A XP_006719924.1:n.559+15G>A
XM_006719861.3:c.559+15G>A XP_006719924.1:n.559+15G>A
XM_024449397.1:c.505+15G>A XP_024305165.1:n.505+15G>A
NM_000231.3:c.505+15G>A MANE Select NP_000222.2:n.505+15G>A
NM_001378244.1:c.559+15G>A NP_001365173.1:n.559+15G>A
NM_001378245.1:c.505+15G>A NP_001365174.1:n.505+15G>A
NM_001378246.1:c.505+15G>A NP_001365175.1:n.505+15G>A
Search 100 bp 5'
Search 100 bp 3'