Canonical Allele Identifier: CA571115598
Gene:

Linked Data

dbSNP Id: rs1277988216
gnomAD v2: 6-151948410-T-C
gnomAD v3: 6-151627275-T-C
gnomAD v4: 6-151627275-T-C
MyVariant Identifiers: chr6:g.151948410T>C (hg19) chr6:g.151627275T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151627275T>C , CM000668.2:g.151627275T>C GRCh38
NC_000006.11:g.151948410T>C , CM000668.1:g.151948410T>C GRCh37
NC_000006.10:g.151990103T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943113.1:n.701T>C
XR_943115.1:n.701T>C
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