Canonical Allele Identifier: CA1949566001

Gene: HBD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5234465T= , CM000673.2:g.5234465T=	GRCh38
NC_000011.9:g.5255695T= , CM000673.1:g.5255695T=	GRCh37
NC_000011.8:g.5212271T=	NCBI36
NG_000007.3:g.63151A=
NG_063112.2:g.14193A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000643122.1:c.-28-4A=	ENSP00000494708.1:n.-28-4A=
ENST00000650601.1:c.-32A= MANE Select	ENSP00000497529.1:n.-32A=
ENST00000292901.7:c.-32A=	ENSP00000292901.3:n.-32A=
ENST00000380299.3:c.-32A=	ENSP00000369654.3:n.-32A=
ENST00000417377.1:c.-32A=	ENSP00000414741.1:n.-32A=
ENST00000429817.1:c.-32A=	ENSP00000393810.1:n.-32A=
NM_000519.3:c.-32A=	NP_000510.1:n.-32A=
NM_000519.4:c.-32A= MANE Select	NP_000510.1:n.-32A=