Canonical Allele Identifier: CA571581156
Gene:

Linked Data

dbSNP Id: rs1323338710
gnomAD v2: 6-156133822-T-C
gnomAD v3: 6-155812688-T-C
gnomAD v4: 6-155812688-T-C
MyVariant Identifiers: chr6:g.156133822T>C (hg19) chr6:g.155812688T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812688T>C , CM000668.2:g.155812688T>C GRCh38
NC_000006.11:g.156133822T>C , CM000668.1:g.156133822T>C GRCh37
NC_000006.10:g.156175514T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19269T>C
XR_943146.1:n.645-649A>G
XR_001744423.1:n.699-649A>G
XR_001744424.1:n.79+19269T>C
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