Canonical Allele Identifier: CA150159506
Gene:

Linked Data

dbSNP Id: rs540786447
gnomAD v3: 6-151627324-C-A
gnomAD v4: 6-151627324-C-A
MyVariant Identifiers: chr6:g.151948459C>A (hg19) chr6:g.151627324C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627324C>A , CM000668.2:g.151627324C>A GRCh38
NC_000006.11:g.151948459C>A , CM000668.1:g.151948459C>A GRCh37
NC_000006.10:g.151990152C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943113.1:n.750C>A
XR_943115.1:n.750C>A
Search 100 bp 5'
Search 100 bp 3'