Canonical Allele Identifier: CA439798673

Gene: ALB

Linked Data

• gnomAD v4: 4-73406632-G-C
• MyVariant Identifiers: chr4:g.74272349G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406632G>C , CM000666.2:g.73406632G>C	GRCh38
NC_000004.11:g.74272349G>C , CM000666.1:g.74272349G>C	GRCh37
NC_000004.10:g.74491213G>C	NCBI36
NG_009291.1:g.7378G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.141G>C MANE Select	ENSP00000295897.4:p.Val47=
ENST00000295897.8:c.141G>C	ENSP00000295897.4:p.Val47=
ENST00000401494.7:c.137+1459G>C	ENSP00000384695.3:n.137+1459G>C
ENST00000415165.6:c.137+1459G>C	ENSP00000401820.2:n.137+1459G>C
ENST00000441319.5:c.147G>C	ENSP00000392541.1:p.Val49=
ENST00000476441.6:c.79+2226G>C	ENSP00000423727.1:n.79+2226G>C
ENST00000503124.5:c.-98G>C	ENSP00000421027.1:n.-98G>C
ENST00000509063.5:c.141G>C	ENSP00000422784.1:p.Val47=
ENST00000510166.5:n.177G>C
ENST00000514786.1:n.110G>C
ENST00000515133.5:n.182G>C
ENST00000621085.4:c.141G>C	ENSP00000483421.1:p.Val47=
ENST00000621628.4:c.141G>C	ENSP00000480485.1:p.Val47=
NM_000477.5:c.141G>C	NP_000468.1:p.Val47=
NM_000477.6:c.141G>C	NP_000468.1:p.Val47=
NM_000477.7:c.141G>C MANE Select	NP_000468.1:p.Val47=