Canonical Allele Identifier: CA55082009
Gene:

Linked Data

dbSNP Id: rs757044593
gnomAD v2: 2-123641449-ATGTTGAATTCTC-A
gnomAD v3: 2-122883873-ATGTTGAATTCTC-A
gnomAD v4: 2-122883873-ATGTTGAATTCTC-A
MyVariant Identifiers: chr2:g.123641450_123641461del (hg19) chr2:g.122883874_122883885del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883876_122883887del , CM000664.2:g.122883876_122883887del GRCh38
NC_000002.11:g.123641452_123641463del , CM000664.1:g.123641452_123641463del GRCh37
NC_000002.10:g.123357922_123357933del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-1066_1125-1055del
XR_001739692.1:n.1451-1066_1451-1055del
XR_923292.2:n.1358-1066_1358-1055del
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