Canonical Allele Identifier: CA1913040868
Gene:

Linked Data

dbSNP Id: rs7085387

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.58444842G>C , CM000672.2:g.58444842G>C GRCh38
NC_000010.10:g.60204602G>C , CM000672.1:g.60204602G>C GRCh37
NC_000010.9:g.59874608G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945981.1:n.356+9185G>C
XR_945982.1:n.356+9185G>C
XR_945983.1:n.356+9185G>C
XR_945984.1:n.112+10801G>C
XR_945985.1:n.73+8636G>C
XR_945986.1:n.356+9185G>C
XR_945981.2:n.360+9185G>C
XR_945982.2:n.360+9185G>C
XR_945983.2:n.360+9185G>C
XR_945984.2:n.116+10801G>C
XR_945985.2:n.73+8636G>C