Canonical Allele Identifier: CA136302089
Gene: CASC15 HGNC NCBI
NBAT1 HGNC NCBI

Linked Data

dbSNP Id: rs910705117
gnomAD v2: 6-22140103-TTC-T
gnomAD v3: 6-22139874-TTC-T
gnomAD v4: 6-22139874-TTC-T
MyVariant Identifiers: chr6:g.22140104_22140105del (hg19) chr6:g.22139875_22139876del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.22139876_22139877del , CM000668.2:g.22139876_22139877del GRCh38
NC_000006.11:g.22140105_22140106del , CM000668.1:g.22140105_22140106del GRCh37
NC_000006.10:g.22248084_22248085del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015410.1:n.1391+28956_1391+28957del (CASC15)
NR_034143.1:n.228-3207_228-3206del (NBAT1)
NR_015410.2:n.1422+28956_1422+28957del (CASC15)
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