Canonical Allele Identifier: CA1610208167
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10886716C>A , CM000668.2:g.10886716C>A GRCh38
NC_000006.11:g.10886949C>A , CM000668.1:g.10886949C>A GRCh37
NC_000006.10:g.10994935C>A NCBI36
NG_008970.1:g.150G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000480294.1:c.101-4797C>A ENSP00000417929.1:n.101-4797C>A