Canonical Allele Identifier: CA595318356
Gene:

Linked Data

dbSNP Id: rs1250279126

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762544C>G , CM000672.2:g.94762544C>G GRCh38
NC_000010.10:g.96522301C>G , CM000672.1:g.96522301C>G GRCh37
NC_000010.9:g.96512291C>G NCBI36
NG_008384.2:g.4839C>G
NG_008384.3:g.4864C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12514C>G ENSP00000483243.1:n.932-12514C>G