Canonical Allele Identifier: CA1605794984
Gene:

Linked Data

dbSNP Id: rs953871231

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535562C>G , CM000668.2:g.1535562C>G GRCh38
NC_000006.11:g.1535797C>G , CM000668.1:g.1535797C>G GRCh37
NC_000006.10:g.1480796C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427861.2:n.234+16784G>C
XR_926380.1:n.218-2894C>G
XR_926381.1:n.1108-2894C>G
XR_926382.1:n.235-6383G>C
XR_926384.1:n.200-6383G>C
XR_001743921.1:n.235-6407G>C
XR_427861.3:n.234+16784G>C
XR_926381.2:n.1123-2894C>G