Canonical Allele Identifier: CA1095587986
Gene: SAMD5 HGNC NCBI

Linked Data

gnomAD v3: 6-147796101-T-TTTTTTTCTTTTTTTTTCTC
gnomAD v4: 6-147796101-T-TTTTTTTCTTTTTTTTTCTC
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147796102_147796103insTTTTTCTTTTTTTTTCTCT , CM000668.2:g.147796102_147796103insTTTTTCTTTTTTTTTCTCT GRCh38
NC_000006.11:g.148117238_148117239insTTTTTCTTTTTTTTTCTCT , CM000668.1:g.148117238_148117239insTTTTTCTTTTTTTTTCTCT GRCh37
NC_000006.10:g.148158931_148158932insTTTTTCTTTTTTTTTCTCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151370_460-151369insTTTTTCTTTTTTTTTCTCT XP_016866339.1:n.460-151370_460-151369insTTTTTCTTTTTTTTTCTCT
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