Canonical Allele Identifier: CA1035793636
Gene:

Linked Data

dbSNP Id: rs1678946382

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368825T>C , CM000664.2:g.122368825T>C GRCh38
NC_000002.11:g.123126401T>C , CM000664.1:g.123126401T>C GRCh37
NC_000002.10:g.122842871T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24138T>C
XR_001739684.1:n.556-24138T>C