Canonical Allele Identifier: CA2632821140
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31090815G>A , CM000678.2:g.31090815G>A GRCh38
NC_000016.9:g.31102136G>A , CM000678.1:g.31102136G>A GRCh37
NC_000016.8:g.31009637G>A NCBI36
NG_011564.1:g.9141C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529564.1:c.283+2497C>T ENSP00000431371.1:n.283+2497C>T
ENST00000532364.1:c.173+3742C>T ENSP00000460316.1:n.173+3742C>T
ENST00000533518.5:c.407+277C>T