Canonical Allele Identifier: CA1010578416
Gene:

Linked Data

dbSNP Id: rs1665421636

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800584_192800585insA , CM000663.2:g.192800584_192800585insA GRCh38
NC_000001.10:g.192769714_192769715insA , CM000663.1:g.192769714_192769715insA GRCh37
NC_000001.9:g.191036337_191036338insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.14_15insA