Canonical Allele Identifier: CA1069047623
Gene:

Linked Data

dbSNP Id: rs1733821980

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559299A>C , CM000666.2:g.144559299A>C GRCh38
NC_000004.11:g.145480451A>C , CM000666.1:g.145480451A>C GRCh37
NC_000004.10:g.145699901A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143321T>G ENSP00000497507.1:n.328-143321T>G
XR_939272.1:n.178+2685T>G
XR_939273.1:n.178+2685T>G
XR_939272.2:n.522+2685T>G
XR_939273.2:n.522+2685T>G