Canonical Allele Identifier: CA12187851
Gene: LTA HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.31572364A>C
GRCh37 chr6:g.31540141A>C
gnomAD v2:
6:31540141 A / C
gnomAD v3:
6:31572364 A / C
gnomAD v4:
chr6-31572364-A-C
Joint Max Group AF 0.73001428 (AFR)
Genomes Max Group AF 0.72970046 (AFR)
Exomes Max Group AF 0.71736162 (AFR)
dbSNP:
2239704
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31572364A>C , CM000668.2:g.31572364A>C GRCh38
NC_000006.11:g.31540141A>C , CM000668.1:g.31540141A>C GRCh37
NC_000006.10:g.31648120A>C NCBI36
NG_007462.1:g.1792A>C
NG_012010.1:g.5266A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000418386.3:c.-92A>C MANE Select ENSP00000413450.2:n.-92A>C
ENST00000418386.2:c.-92A>C ENSP00000413450.2:n.-92A>C
ENST00000454783.5:c.-10+62A>C ENSP00000403495.1:n.-10+62A>C
ENST00000471842.1:n.71A>C
ENST00000489638.5:n.33+62A>C
NM_000595.3:c.-92A>C NP_000586.2:n.-92A>C
NM_001159740.2:c.-10+62A>C NP_001153212.1:n.-10+62A>C
XM_011514614.1:c.-10+62A>C XP_011512916.1:n.-10+62A>C
XM_011514615.1:c.-10+62A>C XP_011512917.1:n.-10+62A>C
XM_011514616.1:c.-10+62A>C XP_011512918.1:n.-10+62A>C
XM_011514617.1:c.-10+62A>C XP_011512919.1:n.-10+62A>C
XM_011514618.1:c.-10+62A>C XP_011512920.1:n.-10+62A>C
XR_926695.1:n.116+219T>G
NR_149045.1:n.121+219T>G
XM_011514615.2:c.-10+62A>C XP_011512917.1:n.-10+62A>C
XM_011514616.2:c.-10+62A>C XP_011512918.1:n.-10+62A>C
XM_011514617.2:c.-10+62A>C XP_011512919.1:n.-10+62A>C
NM_000595.4:c.-92A>C MANE Select NP_000586.2:n.-92A>C
Search 100 bp 5'
Search 100 bp 3'