Canonical Allele Identifier: CA357244206

Gene: ALB

Linked Data

• dbSNP Id: rs1208592979
• gnomAD v2: 4-74283836-T-C
• MyVariant Identifiers: chr4:g.74283836T>C (hg19) ; chr4:g.73418119T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418119T>C , CM000666.2:g.73418119T>C	GRCh38
NC_000004.11:g.74283836T>C , CM000666.1:g.74283836T>C	GRCh37
NC_000004.10:g.74502700T>C	NCBI36
NG_009291.1:g.18865T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1460T>C MANE Select	ENSP00000295897.4:p.Leu487Ser
ENST00000295897.8:c.1460T>C	ENSP00000295897.4:p.Leu487Ser
ENST00000401494.7:c.1115T>C	ENSP00000384695.3:p.Leu372Ser
ENST00000415165.6:c.884T>C	ENSP00000401820.2:p.Leu295Ser
ENST00000476441.6:c.*739T>C	ENSP00000423727.1:n.*739T>C
ENST00000486939.1:n.114T>C
ENST00000503124.5:c.1010T>C	ENSP00000421027.1:p.Leu337Ser
ENST00000505649.5:n.1007T>C
ENST00000509063.5:c.1460T>C	ENSP00000422784.1:p.Leu487Ser
ENST00000511370.1:c.993T>C
ENST00000621085.4:c.821T>C	ENSP00000483421.1:p.Leu274Ser
ENST00000621628.4:c.821T>C	ENSP00000480485.1:p.Leu274Ser
NM_000477.5:c.1460T>C	NP_000468.1:p.Leu487Ser
NM_000477.6:c.1460T>C	NP_000468.1:p.Leu487Ser
NM_000477.7:c.1460T>C MANE Select	NP_000468.1:p.Leu487Ser