Canonical Allele Identifier: CA2756287196
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53056924A>C , CM000665.2:g.53056924A>C GRCh38
NC_000003.11:g.53090940A>C , CM000665.1:g.53090940A>C GRCh37
NC_000003.10:g.53065980A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9685T>G
ENST00000607283.5:c.465-13670T>G
ENST00000607495.5:c.447+20764T>G