Canonical Allele Identifier: CA2504260273
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8734265A>C , CM000686.2:g.8734265A>C GRCh38
NC_000024.9:g.8602306A>C , CM000686.1:g.8602306A>C GRCh37
NC_000024.8:g.8662306A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000623558.1:c.197-5565A>C ENSP00000485446.1:n.197-5565A>C
ENST00000624237.1:c.64-7790A>C ENSP00000485137.1:n.64-7790A>C
ENST00000624593.1:c.-57+14451T>G ENSP00000485106.1:n.-57+14451T>G