Canonical Allele Identifier: CA1041166120
Gene:

Linked Data

dbSNP Id: rs2077889483

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033300A>G , CM000664.2:g.200033300A>G GRCh38
NC_000002.11:g.200898023A>G , CM000664.1:g.200898023A>G GRCh37
NC_000002.10:g.200606268A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22404T>C