Canonical Allele Identifier: CA170719
Gene:

Linked Data

ClinVar Variation Id: 155877
ClinVar RCV Id: RCV000143994 RCV001777152
dbSNP Id: rs2046210
gnomAD v2: 6-151948366-G-A
gnomAD v3: 6-151627231-G-A
gnomAD v4: 6-151627231-G-A
MyVariant Identifiers: chr6:g.151948366G>A (hg19) chr6:g.151627231G>A (hg38)
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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'