Canonical Allele Identifier: CA821226195
Gene:

Linked Data

dbSNP Id: rs1353194261
MyVariant Identifiers: chr6:g.156138687C>A (hg19) chr6:g.155817553C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817553C>A , CM000668.2:g.155817553C>A GRCh38
NC_000006.11:g.156138687C>A , CM000668.1:g.156138687C>A GRCh37
NC_000006.10:g.156180379C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24134C>A
XR_943146.1:n.552-2883G>T
XR_001744423.1:n.606-2883G>T
XR_001744424.1:n.79+24134C>A
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