Canonical Allele Identifier: CA2691985601
Gene:

Linked Data

gnomAD v4: 9-128945526-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128945526G>T , CM000671.2:g.128945526G>T GRCh38
NC_000009.11:g.131707805G>T , CM000671.1:g.131707805G>T GRCh37
NC_000009.10:g.130747626G>T NCBI36
NG_017009.1:g.7208C>A , LRG_744:g.7208C>A
NG_033111.1:g.2834G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000482796.1:c.39-3663G>T ENSP00000417556.2:n.39-3663G>T
Search 100 bp 5'
Search 100 bp 3'