Canonical Allele Identifier: CA604367408
Gene:

Linked Data

dbSNP Id: rs1360223693

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29960973T>C , CM000674.2:g.29960973T>C GRCh38
NC_000012.11:g.30113906T>C , CM000674.1:g.30113906T>C GRCh37
NC_000012.10:g.30005173T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931473.1:n.314-17933A>G
XR_931474.1:n.314-17933A>G
XR_931475.1:n.135-17933A>G
XR_001749060.1:n.314-17933A>G
XR_001749061.1:n.314-17933A>G