Canonical Allele Identifier: CA16841577
Gene:

Linked Data

dbSNP Id: rs879585833

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036365G>C , CM000663.2:g.2036365G>C GRCh38
NC_000001.10:g.1967804G>C , CM000663.1:g.1967804G>C GRCh37
NC_000001.9:g.1957664G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.773+70C>G
XR_001737845.2:n.846C>G
XR_946823.3:n.776+70C>G