Canonical Allele Identifier: CA1504648252
Gene:

Linked Data

dbSNP Id: rs1743707649

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.153943628G>C , CM000666.2:g.153943628G>C GRCh38
NC_000004.11:g.154864780G>C , CM000666.1:g.154864780G>C GRCh37
NC_000004.10:g.155084230G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741892.1:n.1348-5193G>C