Canonical Allele Identifier: CA1674890139
Gene:

Linked Data

dbSNP Id: rs1778927929

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817492A>G , CM000668.2:g.155817492A>G GRCh38
NC_000006.11:g.156138626A>G , CM000668.1:g.156138626A>G GRCh37
NC_000006.10:g.156180318A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24073A>G
XR_943146.1:n.552-2822T>C
XR_001744423.1:n.606-2822T>C
XR_001744424.1:n.79+24073A>G