Canonical Allele Identifier: CA2065107290
Gene:

Linked Data

dbSNP Id: rs1876321334

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398628A>G , CM000674.2:g.115398628A>G GRCh38
NC_000012.11:g.115836433A>G , CM000674.1:g.115836433A>G GRCh37
NC_000012.10:g.114320816A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945389.1:n.697+8467T>C
XR_945389.2:n.701+8467T>C