Canonical Allele Identifier: CA785691739

Gene:

Linked Data

• dbSNP Id: rs1444793517
• MyVariant Identifiers: chr4:g.11503539A>T (hg19) ; chr4:g.11501915A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.11501915A>T , CM000666.2:g.11501915A>T	GRCh38
NC_000004.11:g.11503539A>T , CM000666.1:g.11503539A>T	GRCh37
NC_000004.10:g.11112637A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001741361.1:n.950+19069A>T