Canonical Allele Identifier: CA15632877
Gene:

Linked Data

dbSNP Id: rs7897654

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102902701T>C , CM000672.2:g.102902701T>C GRCh38
NC_000010.10:g.104662458T>C , CM000672.1:g.104662458T>C GRCh37
NC_000010.9:g.104652448T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017017027.1:c.447-2191A>G XP_016872516.1:n.447-2191A>G
XR_001747577.1:n.169-2191A>G
XR_001747578.1:n.345-2191A>G
NR_160733.1:n.169-2191A>G