Canonical Allele Identifier: CA357245054

Gene: ALB

Linked Data

• dbSNP Id: rs2149329631
• MyVariant Identifiers: chr4:g.74283971C>G (hg19) ; chr4:g.73418254C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418254C>G , CM000666.2:g.73418254C>G	GRCh38
NC_000004.11:g.74283971C>G , CM000666.1:g.74283971C>G	GRCh37
NC_000004.10:g.74502835C>G	NCBI36
NG_009291.1:g.19000C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1595C>G MANE Select	ENSP00000295897.4:p.Thr532Ser
ENST00000295897.8:c.1595C>G	ENSP00000295897.4:p.Thr532Ser
ENST00000401494.7:c.1250C>G	ENSP00000384695.3:p.Thr417Ser
ENST00000415165.6:c.1019C>G	ENSP00000401820.2:p.Thr340Ser
ENST00000476441.6:c.*874C>G	ENSP00000423727.1:n.*874C>G
ENST00000486939.1:n.249C>G
ENST00000503124.5:c.1145C>G	ENSP00000421027.1:p.Thr382Ser
ENST00000505649.5:n.1142C>G
ENST00000509063.5:c.1595C>G	ENSP00000422784.1:p.Thr532Ser
ENST00000511370.1:c.1128C>G
ENST00000621085.4:c.956C>G	ENSP00000483421.1:p.Thr319Ser
ENST00000621628.4:c.956C>G	ENSP00000480485.1:p.Thr319Ser
NM_000477.5:c.1595C>G	NP_000468.1:p.Thr532Ser
NM_000477.6:c.1595C>G	NP_000468.1:p.Thr532Ser
NM_000477.7:c.1595C>G MANE Select	NP_000468.1:p.Thr532Ser