Canonical Allele Identifier: CA2674237916
Gene: HEXB HGNC NCBI

Linked Data

gnomAD v4: 5-74685662-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.74685662A>C , CM000667.2:g.74685662A>C GRCh38
NC_000005.9:g.73981487A>C , CM000667.1:g.73981487A>C GRCh37
NC_000005.8:g.74017243A>C NCBI36
NG_009770.1:g.5519A>C
NG_009770.2:g.50640A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261416.12:c.299+103A>C MANE Select ENSP00000261416.7:n.299+103A>C
ENST00000261416.11:c.299+103A>C ENSP00000261416.7:n.299+103A>C
ENST00000511181.5:c.-376-3666A>C ENSP00000426285.1:n.-376-3666A>C
ENST00000513079.5:n.364+103A>C
ENST00000515528.1:n.354+103A>C
NM_000521.3:c.299+103A>C NP_000512.1:n.299+103A>C
NM_001292004.1:c.-376-3666A>C NP_001278933.1:n.-376-3666A>C
NM_000521.4:c.299+103A>C MANE Select NP_000512.2:n.299+103A>C
NM_001292004.2:c.-376-3666A>C NP_001278933.1:n.-376-3666A>C
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