Canonical Allele Identifier: CA1035793692
Gene:

Linked Data

dbSNP Id: rs1678947514

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368922C>T , CM000664.2:g.122368922C>T GRCh38
NC_000002.11:g.123126498C>T , CM000664.1:g.123126498C>T GRCh37
NC_000002.10:g.122842968C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24041C>T
XR_001739684.1:n.556-24041C>T