Canonical Allele Identifier: CA821223663
Gene:

Linked Data

dbSNP Id: rs1432211774
gnomAD v3: 6-155812625-T-C
gnomAD v4: 6-155812625-T-C
MyVariant Identifiers: chr6:g.156133759T>C (hg19) chr6:g.155812625T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812625T>C , CM000668.2:g.155812625T>C GRCh38
NC_000006.11:g.156133759T>C , CM000668.1:g.156133759T>C GRCh37
NC_000006.10:g.156175451T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19206T>C
XR_943146.1:n.645-586A>G
XR_001744423.1:n.699-586A>G
XR_001744424.1:n.79+19206T>C
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