Canonical Allele Identifier: CA1697889700
Gene:

Linked Data

dbSNP Id: rs1790896044

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897484_30897487del , CM000669.2:g.30897484_30897487del GRCh38
NC_000007.13:g.30937099_30937102del , CM000669.1:g.30937099_30937102del GRCh37
NC_000007.12:g.30903624_30903627del NCBI36
NG_007475.2:g.49091_49094del

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.621+14491_621+14494del