Canonical Allele Identifier: CA2670966860

Gene: ALB

Linked Data

• gnomAD v4: 4-73420440-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420440T>C , CM000666.2:g.73420440T>C	GRCh38
NC_000004.11:g.74286157T>C , CM000666.1:g.74286157T>C	GRCh37
NC_000004.10:g.74505021T>C	NCBI36
NG_009291.1:g.21186T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.*23+119T>C MANE Select	ENSP00000295897.4:n.*23+119T>C
ENST00000295897.8:c.*23+119T>C	ENSP00000295897.4:n.*23+119T>C
ENST00000401494.7:c.*23+119T>C	ENSP00000384695.3:n.*23+119T>C
ENST00000415165.6:c.*23+119T>C	ENSP00000401820.2:n.*23+119T>C
ENST00000476441.6:c.*1132+119T>C	ENSP00000423727.1:n.*1132+119T>C
ENST00000495173.1:n.161+119T>C
ENST00000503124.5:c.*23+119T>C	ENSP00000421027.1:n.*23+119T>C
ENST00000505649.5:n.1400+119T>C
ENST00000508932.5:n.243+119T>C
ENST00000509063.5:c.1786-652T>C	ENSP00000422784.1:n.1786-652T>C
ENST00000511370.1:c.1386+119T>C
ENST00000621085.4:c.*23+119T>C	ENSP00000483421.1:n.*23+119T>C
ENST00000621628.4:c.*23+119T>C	ENSP00000480485.1:n.*23+119T>C
NM_000477.5:c.*23+119T>C	NP_000468.1:n.*23+119T>C
NM_000477.6:c.*23+119T>C	NP_000468.1:n.*23+119T>C
NM_000477.7:c.*23+119T>C MANE Select	NP_000468.1:n.*23+119T>C