Canonical Allele Identifier: CA974703393
Gene: BCAR4 HGNC NCBI

Linked Data

dbSNP Id: rs4561483

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11826180A>C , CM000678.2:g.11826180A>C GRCh38
NC_000016.9:g.11920037A>C , CM000678.1:g.11920037A>C GRCh37
NC_000016.8:g.11827538A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024049.1:n.512-1441T>G
NR_024050.1:n.204+2142T>G
NR_131216.1:n.134+2519T>G
NR_131217.1:n.419+2142T>G
NR_131222.1:n.134+2519T>G