Canonical Allele Identifier: CA357244289

Gene: ALB

Linked Data

• dbSNP Id: rs1719063247
• MyVariant Identifiers: chr4:g.74283854T>C (hg19) ; chr4:g.73418137T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418137T>C , CM000666.2:g.73418137T>C	GRCh38
NC_000004.11:g.74283854T>C , CM000666.1:g.74283854T>C	GRCh37
NC_000004.10:g.74502718T>C	NCBI36
NG_009291.1:g.18883T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1478T>C MANE Select	ENSP00000295897.4:p.Val493Ala
ENST00000295897.8:c.1478T>C	ENSP00000295897.4:p.Val493Ala
ENST00000401494.7:c.1133T>C	ENSP00000384695.3:p.Val378Ala
ENST00000415165.6:c.902T>C	ENSP00000401820.2:p.Val301Ala
ENST00000476441.6:c.*757T>C	ENSP00000423727.1:n.*757T>C
ENST00000486939.1:n.132T>C
ENST00000503124.5:c.1028T>C	ENSP00000421027.1:p.Val343Ala
ENST00000505649.5:n.1025T>C
ENST00000509063.5:c.1478T>C	ENSP00000422784.1:p.Val493Ala
ENST00000511370.1:c.1011T>C
ENST00000621085.4:c.839T>C	ENSP00000483421.1:p.Val280Ala
ENST00000621628.4:c.839T>C	ENSP00000480485.1:p.Val280Ala
NM_000477.5:c.1478T>C	NP_000468.1:p.Val493Ala
NM_000477.6:c.1478T>C	NP_000468.1:p.Val493Ala
NM_000477.7:c.1478T>C MANE Select	NP_000468.1:p.Val493Ala