Canonical Allele Identifier: CA150159464
Gene:

Linked Data

dbSNP Id: rs950189607
gnomAD v2: 6-151948425-T-C
gnomAD v3: 6-151627290-T-C
gnomAD v4: 6-151627290-T-C
MyVariant Identifiers: chr6:g.151948425T>C (hg19) chr6:g.151627290T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627290T>C , CM000668.2:g.151627290T>C GRCh38
NC_000006.11:g.151948425T>C , CM000668.1:g.151948425T>C GRCh37
NC_000006.10:g.151990118T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943113.1:n.716T>C
XR_943115.1:n.716T>C
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