Canonical Allele Identifier: CA1369169894
Gene:

Linked Data

dbSNP Id: rs2041753453

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428161T>C , CM000665.2:g.61428161T>C GRCh38
NC_000003.11:g.61413835T>C , CM000665.1:g.61413835T>C GRCh37
NC_000003.10:g.61388875T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.164+353A>G
XR_940893.1:n.164+353A>G
XR_001740725.1:n.202+353A>G
XR_940892.2:n.202+353A>G