Canonical Allele Identifier: CA2572018529
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762557T>C , CM000672.2:g.94762557T>C GRCh38
NC_000010.10:g.96522314T>C , CM000672.1:g.96522314T>C GRCh37
NC_000010.9:g.96512304T>C NCBI36
NG_008384.2:g.4852T>C
NG_008384.3:g.4877T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-12501T>C ENSP00000483243.1:n.932-12501T>C