Canonical Allele Identifier: CA170719
Gene:
COSMIC:
COSN17133179 (not active)
COSN17134006 (not active)
COSN17134892 (not active)
COSN17136656 (not active)
COSN17138570 (not active)
COSN17139490 (not active)
COSN17141207 (not active)
COSN17143451 (not active)
COSN17145225 (not active)
COSN17147927 (not active)
COSN17151621 (not active)
COSN17152623 (not active)
MyVariant.info:
GRCh38 chr6:g.151627231G>A
GRCh37 chr6:g.151948366G>A
gnomAD v2:
6:151948366 G / A
gnomAD v3:
6:151627231 G / A
gnomAD v4:
chr6-151627231-G-A
Joint Max Group AF 0.61469368 (AFR)
Genomes Max Group AF 0.61469368 (AFR)
ClinVar RCV:
RCV000143994
RCV001777152
ClinVar Variation:
155877
dbSNP:
2046210
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627231G>A , CM000668.2:g.151627231G>A GRCh38
NC_000006.11:g.151948366G>A , CM000668.1:g.151948366G>A GRCh37
NC_000006.10:g.151990059G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943113.1:n.657G>A
XR_943115.1:n.657G>A
Search 100 bp 5'
Search 100 bp 3'