Canonical Allele Identifier: CA2511331176
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166894T>C , CM000673.2:g.112166894T>C GRCh38
NC_000011.9:g.112037617T>C , CM000673.1:g.112037617T>C GRCh37
NC_000011.8:g.111542827T>C NCBI36
NG_028143.1:g.2224A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000525987.5:n.320-3525T>C
ENST00000531744.5:c.315-3525T>C ENSP00000456957.1:n.315-3525T>C
ENST00000532699.1:c.315-3525T>C ENSP00000456434.1:n.315-3525T>C