Canonical Allele Identifier: CA2722523235
Gene:

Linked Data

dbSNP Id: rs2134226763

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762473A>G , CM000672.2:g.94762473A>G GRCh38
NC_000010.10:g.96522230A>G , CM000672.1:g.96522230A>G GRCh37
NC_000010.9:g.96512220A>G NCBI36
NG_008384.2:g.4768A>G
NG_008384.3:g.4793A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12585A>G ENSP00000483243.1:n.932-12585A>G