Canonical Allele Identifier: CA2211402908
Community Standard Title: NC_000016.10:g.19144694G=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.19144694G= , CM000678.2:g.19144694G= GRCh38
NC_000016.9:g.19156016G= , CM000678.1:g.19156016G= GRCh37
NC_000016.8:g.19063517G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000564808.6:c.642+17409G=
ENST00000568526.1:c.212-8394G=